| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90211614-90211944 | Common:4; Rare:101 | ||||
| chr7:90245083-90245258 | Common:1; Rare:56 | ||||
| chr7:90346603-90346744 | Common:4; Rare:64 | ||||
| chr7:90595887-90596027 | Common:6; Rare:53 | ||||
| chr7:90596248-90596480 | Rare:75 | ||||
| chr7:91880658-91880820 | Common:1; Rare:46 | ||||
| chr7:91940827-91941002 | Common:3; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134432-92134577 | Rare:46 | ||||
| chr7:92134773-92134854 | Common:2; Rare:22 | ||||
| chr7:92245658-92245997 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:92528328-92528815 | Common:3; Rare:147; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232201-93232390 | Common:2; Rare:34 | ||||
| chr7:93921966-93922182 | Common:4; Rare:61 | ||||
| chr7:94425743-94426050 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94598952-94599108 | Rare:35; Clinvar:2; Clinvar (benign):1 |