| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5781589-5781809 | Common:1; Rare:93 | ||||
| chr7:6009015-6009383 | Common:4; Rare:156; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr7:6009467-6009608 | Common:3; Rare:65 | ||||
| chr7:6031252-6031411 | Rare:26 | ||||
| chr7:6104622-6105002 | Common:5; Rare:135 | ||||
| chr7:6272478-6272727 | Rare:108 | ||||
| chr7:6348719-6349076 | Common:7; Rare:173 | ||||
| chr7:6400051-6400183 | Rare:30 | ||||
| chr7:6447946-6448071 | Common:1; Rare:41 | ||||
| chr7:6483981-6484240 | Common:2; Rare:121 | ||||
| chr7:6706929-6707129 | Common:2; Rare:80 | ||||
| chr7:7182344-7182683 | Common:4; Rare:127 | ||||
| chr7:7566752-7567037 | Common:5; Rare:121 | ||||
| chr7:7968560-7968742 | Rare:61 | ||||
| chr7:8262120-8262294 | Rare:80 |