| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152025510-152025775 | Common:1; Rare:104 | ||||
| chr7:152676096-152676295 | Common:2; Rare:84; Clinvar (benign):6 | ||||
| chr7:155002933-155003010 | Rare:23 | ||||
| chr7:155644349-155644724 | Common:2; Rare:131 | ||||
| chr7:156640556-156640700 | Common:2; Rare:77 | ||||
| chr7:157336790-157337138 | Common:3; Rare:158; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158856425-158856677 | Common:6; Rare:92 | ||||
| chr8:232180-232452 | Common:3; Rare:111 | ||||
| chr8:233032-233094 | Rare:15 | ||||
| chr8:406717-406985 | Common:4; Rare:130 | ||||
| chr8:6406527-6406679 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563208-6563442 | Common:1; Rare:57 | ||||
| chr8:6708179-6708286 | Common:2; Rare:42 | ||||
| chr8:11769565-11769774 | Common:5; Rare:88 | ||||
| chr8:11802446-11802792 | Common:6; Rare:187 |