| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151028250-151028490 | Rare:94 | ||||
| chr7:151057878-151058252 | Common:4; Rare:93 | ||||
| chr7:151059472-151059696 | Common:1; Rare:70 | ||||
| chr7:151232411-151232528 | Rare:38 | ||||
| chr7:151341515-151341835 | Common:4; Rare:99 | ||||
| chr7:151408987-151409267 | Common:1; Rare:71 | ||||
| chr7:151877118-151877525 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152025458-152025802 | Common:1; Rare:127 | ||||
| chr7:152435957-152436266 | Rare:108 | ||||
| chr7:152436503-152436853 | Rare:121 | ||||
| chr7:152676138-152676284 | Common:2; Rare:54 | ||||
| chr7:155002917-155002998 | Rare:28 | ||||
| chr7:155644377-155644746 | Common:2; Rare:127 | ||||
| chr7:156640535-156640692 | Common:3; Rare:83 | ||||
| chr7:157336790-157337090 | Common:3; Rare:140; Clinvar:3; Clinvar (benign):1 |