| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130440977-130441306 | Common:3; Rare:138; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:131109745-131110142 | Common:1; Rare:76 | ||||
| chr7:131327688-131327909 | Rare:67 | ||||
| chr7:134316713-134317207 | Common:2; Rare:136 | ||||
| chr7:134459045-134459274 | Common:3; Rare:103 | ||||
| chr7:134646553-134646889 | Common:7; Rare:110 | ||||
| chr7:134779579-134779680 | Rare:18 | ||||
| chr7:134891322-134891665 | Common:3; Rare:91 | ||||
| chr7:134986379-134986562 | Common:4; Rare:69 | ||||
| chr7:135147998-135148185 | Rare:42 | ||||
| chr7:135170645-135170986 | Common:6; Rare:110 | ||||
| chr7:135211468-135211738 | Common:2; Rare:133 | ||||
| chr7:135510056-135510277 | Common:3; Rare:50 | ||||
| chr7:135557655-135557947 | Common:3; Rare:82 | ||||
| chr7:135662341-135662548 | Common:4; Rare:92 |