| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152676043-152676277 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):13 | ||||
| chr7:155003122-155003512 | Common:7; Rare:140 | ||||
| chr7:155644355-155644908 | Common:6; Rare:179 | ||||
| chr7:156640531-156640693 | Common:3; Rare:88 | ||||
| chr7:156893154-156893374 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:156949632-156949783 | Rare:54 | ||||
| chr7:157009325-157009464 | Common:1; Rare:33 | ||||
| chr7:157010619-157010949 | Common:5; Rare:102 | ||||
| chr7:157138688-157138988 | Common:2; Rare:94 | ||||
| chr7:157336924-157337016 | Rare:27 | ||||
| chr7:158704729-158704990 | Common:1; Rare:91 | ||||
| chr7:158829470-158829676 | Common:2; Rare:78 | ||||
| chr7:158856415-158856771 | Common:7; Rare:129 | ||||
| chr8:232139-232397 | Common:3; Rare:103 | ||||
| chr8:1755612-1755903 | Common:5; Rare:91 |