| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:7566795-7567037 | Common:4; Rare:101 | ||||
| chr7:8262119-8262256 | Rare:61 | ||||
| chr7:20330776-20331066 | Common:2; Rare:79 | ||||
| chr7:20331328-20331394 | Common:1; Rare:20 | ||||
| chr7:20331739-20331807 | Common:1; Rare:24 | ||||
| chr7:22822707-22822911 | Common:2; Rare:84 | ||||
| chr7:23105673-23105871 | Common:3; Rare:105; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181708-23182120 | Common:2; Rare:145 | ||||
| chr7:23299196-23299382 | Common:2; Rare:94 | ||||
| chr7:23470362-23470543 | Rare:55 | ||||
| chr7:26196557-26196930 | Common:2; Rare:141; Clinvar (benign):1 | ||||
| chr7:26197315-26197681 | Common:1; Rare:124; Clinvar (benign):1 | ||||
| chr7:26201416-26201830 | Common:2; Rare:194 | ||||
| chr7:27130754-27131021 | Common:1; Rare:58 | ||||
| chr7:30594716-30594908 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):4 |