| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139036010-139036188 | Rare:49 | ||||
| chr7:139109338-139109493 | Common:1; Rare:45 | ||||
| chr7:140697107-140697329 | Rare:80 | ||||
| chr7:141551335-141551437 | Rare:28; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738048-141738429 | Common:4; Rare:122 | ||||
| chr7:143380838-143381420 | Common:2; Rare:171 | ||||
| chr7:143388313-143388631 | Common:3; Rare:97 | ||||
| chr7:149147257-149147476 | Common:3; Rare:49 | ||||
| chr7:149261893-149262236 | Common:2; Rare:108 | ||||
| chr7:150368820-150368875 | Rare:15 | ||||
| chr7:150405893-150406147 | Common:1; Rare:48 | ||||
| chr7:151057856-151058205 | Common:3; Rare:99 | ||||
| chr7:151248651-151248824 | Common:1; Rare:50 | ||||
| chr7:151249223-151249320 | Common:1; Rare:19 | ||||
| chr7:155644394-155644716 | Common:2; Rare:108 |