| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:101321729-101321880 | Common:3; Rare:53 | ||||
| chr7:102464846-102464988 | Common:1; Rare:61 | ||||
| chr7:105014087-105014220 | Common:1; Rare:59 | ||||
| chr7:105532070-105532240 | Common:1; Rare:45 | ||||
| chr7:106112200-106112494 | Common:3; Rare:97 | ||||
| chr7:106284837-106285418 | Common:6; Rare:214 | ||||
| chr7:107563892-107564041 | Common:2; Rare:90; Clinvar (benign):5 | ||||
| chr7:107580147-107580306 | Common:2; Rare:61 | ||||
| chr7:107744058-107744164 | Rare:36 | ||||
| chr7:108003008-108003341 | Common:3; Rare:94 | ||||
| chr7:108526099-108526463 | Common:5; Rare:114 | ||||
| chr7:108569592-108569958 | Common:1; Rare:132 | ||||
| chr7:112206418-112206751 | Common:1; Rare:121 | ||||
| chr7:116210390-116210640 | Common:4; Rare:63 |