Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34105701-34105925 | Rare:43 | ||||
chr20:34930980-34931264 | Common:2; Rare:47 | ||||
chr20:34936780-34936982 | Rare:57; Clinvar (pathogenic):1 | ||||
chr20:35183662-35183702 | Rare:4 | ||||
chr20:35263140-35263466 | Common:4; Rare:48 | ||||
chr20:35263522-35263853 | Rare:50 | ||||
chr20:35479712-35479984 | Common:1; Rare:58 | ||||
chr20:35548532-35548839 | Rare:99 | ||||
chr20:35663802-35663850 | Rare:13 | ||||
chr20:35704605-35704733 | Rare:29 | ||||
chr20:36045930-36045946 | |||||
chr20:36048999-36049040 | Rare:11 | ||||
chr20:36050010-36050072 | Rare:8 | ||||
chr20:36050917-36051078 | Common:2; Rare:59 | ||||
chr20:36462249-36462332 | Rare:15 |