| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22818219-22818442 | Rare:40 | ||||
| chr7:22818618-22818668 | Common:3; Rare:12 | ||||
| chr7:22822270-22822391 | Common:1; Rare:24 | ||||
| chr7:22822661-22822975 | Common:3; Rare:115 | ||||
| chr7:23014007-23014341 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105636-23105865 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181757-23182117 | Common:2; Rare:134 | ||||
| chr7:23246629-23246900 | Common:4; Rare:73 | ||||
| chr7:23299193-23299542 | Common:2; Rare:173 | ||||
| chr7:23347671-23347826 | Rare:46 | ||||
| chr7:23347976-23348218 | Rare:34 | ||||
| chr7:23470298-23470624 | Common:1; Rare:97 | ||||
| chr7:23597261-23597567 | Common:1; Rare:92 | ||||
| chr7:24757395-24757626 | Common:2; Rare:70 | ||||
| chr7:24980100-24980441 | Common:8; Rare:138 |