| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:130070281-130070577 | Common:2; Rare:77 | ||||
| chr7:130205384-130205520 | Rare:60 | ||||
| chr7:130266577-130266960 | Rare:93 | ||||
| chr7:130379817-130379886 | Common:1; Rare:8 | ||||
| chr7:130381511-130382223 | Common:4; Rare:222; Clinvar (benign):2 | ||||
| chr7:130383371-130383546 | Rare:57; Clinvar:1 | ||||
| chr7:130384308-130384481 | Common:3; Rare:33 | ||||
| chr7:130384911-130385380 | Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:131109892-131110101 | Common:1; Rare:35 | ||||
| chr7:131327711-131327909 | Rare:65 | ||||
| chr7:134646566-134646856 | Common:6; Rare:83 | ||||
| chr7:134986417-134986560 | Common:4; Rare:58 | ||||
| chr7:135148009-135148107 | Rare:24 | ||||
| chr7:135170665-135170809 | Common:2; Rare:57 | ||||
| chr7:135662357-135662515 | Common:4; Rare:64 |