| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22726206-22726258 | Rare:8 | ||||
| chr7:22727026-22727210 | Rare:13 | ||||
| chr7:23105673-23105976 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181872-23182117 | Rare:102 | ||||
| chr7:23531884-23532041 | Common:2; Rare:62 | ||||
| chr7:24757409-24757550 | Common:1; Rare:45 | ||||
| chr7:24980157-24980414 | Common:8; Rare:107 | ||||
| chr7:25125209-25125643 | Rare:178; Clinvar:3 | ||||
| chr7:26200573-26200941 | Common:1; Rare:180 | ||||
| chr7:26201020-26201555 | Common:1; Rare:212 | ||||
| chr7:26201615-26201800 | Common:1; Rare:100 | ||||
| chr7:26864535-26864840 | Common:3; Rare:94 | ||||
| chr7:27095976-27096229 | Rare:73 | ||||
| chr7:27152533-27152721 | Rare:34 | ||||
| chr7:27172754-27173055 | Rare:74 |