| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2541360-2541738 | Common:4; Rare:150; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr7:4775523-4775718 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:5513746-5513876 | Common:1; Rare:55 | ||||
| chr7:6009029-6009323 | Common:3; Rare:123; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:6104671-6105002 | Common:5; Rare:110 | ||||
| chr7:6447940-6448066 | Common:1; Rare:42 | ||||
| chr7:6706927-6707099 | Rare:69 | ||||
| chr7:7566753-7567054 | Common:5; Rare:125 | ||||
| chr7:8262120-8262287 | Rare:73 | ||||
| chr7:8262512-8262605 | Common:1; Rare:29 | ||||
| chr7:10973776-10973919 | Rare:65 | ||||
| chr7:12403839-12403984 | Common:1; Rare:35 | ||||
| chr7:12686718-12687043 | Common:3; Rare:103 | ||||
| chr7:12687389-12687643 | Common:5; Rare:80 | ||||
| chr7:15396573-15396797 | Common:2; Rare:92 |