| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341197-139341356 | Rare:34 | ||||
| chr7:141551284-141551428 | Common:1; Rare:44; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:149028409-149028549 | Common:2; Rare:54 | ||||
| chr7:155644384-155644730 | Common:2; Rare:116 | ||||
| chr7:157336790-157337061 | Common:2; Rare:123 | ||||
| chr8:6406527-6406668 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:11284741-11284848 | Common:2; Rare:47 | ||||
| chr8:11802440-11802792 | Common:6; Rare:191 | ||||
| chr8:17246826-17246982 | Common:1; Rare:63 | ||||
| chr8:23457624-23457771 | Common:2; Rare:58 | ||||
| chr8:26382972-26383090 | Rare:52 | ||||
| chr8:33485022-33485211 | Common:2; Rare:64 | ||||
| chr8:37762478-37762672 | Common:2; Rare:68 | ||||
| chr8:38176430-38176881 | Common:5; Rare:129 | ||||
| chr8:42541565-42541628 | Rare:18 |