| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:12211191-12211424 | Common:3; Rare:94 | ||||
| chr7:12570709-12570801 | Common:3; Rare:43 | ||||
| chr7:12687422-12687676 | Common:5; Rare:79 | ||||
| chr7:16645690-16646225 | Common:5; Rare:189 | ||||
| chr7:17298444-17298738 | Common:3; Rare:79 | ||||
| chr7:17298881-17299189 | Common:2; Rare:88 | ||||
| chr7:17940398-17940606 | Common:2; Rare:101 | ||||
| chr7:20217324-20217594 | Common:1; Rare:58 | ||||
| chr7:20330657-20331217 | Common:2; Rare:143 | ||||
| chr7:20331719-20331856 | Common:1; Rare:47 | ||||
| chr7:22356126-22356186 | Rare:5 | ||||
| chr7:23105695-23105829 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181891-23182117 | Rare:92 | ||||
| chr7:23470362-23470557 | Rare:58 | ||||
| chr7:24757416-24757626 | Common:1; Rare:63 |