Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47191893-47192076 | Common:2; Rare:36 | ||||
chr2:47422477-47422789 | Common:4; Rare:77 | ||||
chr2:47802561-47802620 | Rare:15 | ||||
chr2:47803159-47803493 | Common:2; Rare:123; Clinvar:22; Clinvar (benign):15 | ||||
chr2:47806072-47806345 | Common:1; Rare:117; Clinvar:35; Clinvar (benign):17; Clinvar (pathogenic):9 | ||||
chr2:47906438-47906818 | Common:2; Rare:145 | ||||
chr2:48315679-48315781 | Rare:34 | ||||
chr2:51350126-51350308 | Rare:36 | ||||
chr2:53795648-53795945 | Common:1; Rare:64 | ||||
chr2:53797516-53797795 | Rare:79 | ||||
chr2:53817671-53817896 | Rare:45 | ||||
chr2:53906670-53906809 | Rare:35 | ||||
chr2:53913484-53913718 | Common:1; Rare:42 | ||||
chr2:53970008-53970192 | Rare:55 | ||||
chr2:54457919-54458025 | Rare:33 |