| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100430215-100430615 | Common:1; Rare:233 | ||||
| chr7:100444275-100444675 | Rare:75 | ||||
| chr7:100444692-100444842 | Common:1; Rare:40 | ||||
| chr7:100450387-100450787 | Rare:126 | ||||
| chr7:100546570-100547345 | Rare:233 | ||||
| chr7:100569628-100569736 | Common:1; Rare:26 | ||||
| chr7:100626613-100626820 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr7:100694100-100694680 | Common:6; Rare:159 | ||||
| chr7:100803550-100803840 | Common:4; Rare:59 | ||||
| chr7:100837378-100837595 | Common:1; Rare:56 | ||||
| chr7:101121930-101122190 | Rare:36 | ||||
| chr7:101138351-101138527 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:101138615-101138730 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:101163041-101163191 | Rare:95 | ||||
| chr7:101282925-101283325 | Common:2; Rare:121 |