Connects human diseases/traits with cell types/tissues based on overlaps between disease-associated genetic variants and cis-regulatory elements. It can be used to retrieve potential disease-causative genetic variants overlapping specific regulatory sequences.
Nikolic M, Papantonis A, Rada-Iglesias A "GARLIC: a bioinformatic toolkit for aetiologically connecting diseases and cell type-specific regulatory maps." Hum. Mol. Genet. 2017; 26(4):742-752 https://doi.org/10.1093/hmg/ddw423
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