Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24310309-24310580 | Rare:79 | ||||
chr2:26254243-26254474 | Common:1; Rare:65; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:26256071-26256327 | Common:1; Rare:42 | ||||
chr2:27025664-27025936 | Common:2; Rare:59 | ||||
chr2:27375338-27375552 | Rare:63 | ||||
chr2:27716693-27716804 | Rare:25 | ||||
chr2:27774171-27774433 | Common:1; Rare:56 | ||||
chr2:30346366-30346754 | Common:4; Rare:82 | ||||
chr2:32947806-32947816 | Common:1; Rare:1 | ||||
chr2:37737565-37737735 | Common:1; Rare:26 | ||||
chr2:47335173-47335319 | Rare:28 | ||||
chr2:47906479-47906885 | Common:2; Rare:142 | ||||
chr2:53808929-53809265 | Rare:90 | ||||
chr2:58056642-58056814 | Rare:36 | ||||
chr2:69582864-69583088 | Common:1; Rare:38 |