ABSTRACT Translating information on genetic risk for body weight regulation into molecular mechanisms can have a significant impact on intervention and therapies. We are seeking to identify genetic variation and their molecular mechanisms that influences obesity through direct effects on the hypothalamus as it is the brain hub that regulates energy homeostasis and there is now considerable evidence for genetic influence to impact this brain region. However, the majority of genetic loci associated with this common, chronic disorder in the general population are located in noncoding regions of the genome, suggesting their influence on energy homeostasis is manifested through changes to the regulome. Thus, pinpointing the causal human variants and connecting them to their downstream targets in brain presents challenges of tissue access for study because much epigenetic control is species-, tissue- and context- specific. To overcome the barrier of limited human tissue access, we have developed a robust protocol for generating human induced pluripotent stem cell (iPSC)- derived neuronal cultures that recapitulate many of the features of hypothalamic neurons from the arcuate nucleus, including by benchmarking this in vitro model to in vivo events that are pivotal in hypothalamic development. We are using this human model and state of the art high throughput assays to map the currently uncharted regulatory landscape of the human hypothalamic neurons across 3 stages in development (early, mid, and late) and under experimental obesogenic conditions. We have published an integrated pipeline to chart the regulatory landscapes of obesity-associated loci within two cell types central to obesity etiology. Next, in order to precisely pinpoint the functional variants in BMI GWAS loci that have influence on body weight regulation through hypothalamic epigenomic regulation, we will identify those that influence chromatin accessibility and/or target gene expression by assay in 30 iPSC-derived hypothalamic-like cellular models generated from subjects of the San Antonio Mexican American Family Studies. GWAS variants with both properties have high potential to be causal and manifest effects on body mass index through changes in chromatin structure. Causal determination will be made for a set of these variants using genome editing techniques such as CRISPR/Cas9 to generate isogenic human neuronal cell lines that differ by genotype only at the single locus. Changes in exon-specific target gene expression and chromatin status will be assessed temporally and under each obesogenic condition. Discovery of epigenetic mechanisms connected to genetic liability will translate the genetic risk information and identify potential underlying factors behind both heritable and diet-induced obesity susceptibility.