Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:10038420-10038597 | Common:2; Rare:32 | ||||
chr7:11298260-11298492 | Common:1; Rare:48 | ||||
chr7:16420623-16420801 | Common:2; Rare:54 | ||||
chr7:20220046-20220322 | Rare:62 | ||||
chr7:21141529-21141739 | Common:2; Rare:39 | ||||
chr7:23285783-23285963 | Common:1; Rare:49 | ||||
chr7:24979478-24979557 | Common:1; Rare:22 | ||||
chr7:25778333-25778613 | Rare:53 | ||||
chr7:25856959-25857273 | Common:12; Rare:91 | ||||
chr7:26193252-26193671 | Rare:146; Clinvar (benign):1 | ||||
chr7:32728756-32728890 | Common:7; Rare:50 | ||||
chr7:32942468-32942650 | Common:1; Rare:50 | ||||
chr7:38341441-38341618 | Common:2; Rare:39 | ||||
chr7:44895029-44895366 | Common:2; Rare:67 | ||||
chr7:44986577-44986742 | Common:3; Rare:80 |