| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645690-16646243 | Common:5; Rare:198 | ||||
| chr7:17298444-17298653 | Common:3; Rare:52 | ||||
| chr7:17940412-17940592 | Common:2; Rare:90 | ||||
| chr7:18509121-18509398 | Rare:50 | ||||
| chr7:20331728-20331780 | Common:1; Rare:17 | ||||
| chr7:21427194-21427544 | Common:5; Rare:119 | ||||
| chr7:21945827-21946161 | Common:3; Rare:107 | ||||
| chr7:22822748-22822963 | Common:3; Rare:82 | ||||
| chr7:23014023-23014380 | Common:5; Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105642-23105829 | Common:4; Rare:99; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181914-23182096 | Rare:79 | ||||
| chr7:23470362-23470569 | Rare:61 | ||||
| chr7:23531948-23532092 | Common:1; Rare:58 | ||||
| chr7:23597281-23597412 | Rare:40 | ||||
| chr7:24757395-24757626 | Common:2; Rare:70 |