| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:12687389-12687636 | Common:5; Rare:79 | ||||
| chr7:16645694-16646202 | Common:3; Rare:178 | ||||
| chr7:17298454-17298659 | Common:3; Rare:49 | ||||
| chr7:17940414-17940574 | Common:1; Rare:83 | ||||
| chr7:20217337-20217598 | Common:1; Rare:56 | ||||
| chr7:20330573-20330742 | Common:2; Rare:42 | ||||
| chr7:20331733-20331784 | Common:1; Rare:16 | ||||
| chr7:23105682-23105833 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181886-23182117 | Rare:93 | ||||
| chr7:24980147-24980377 | Common:6; Rare:92 | ||||
| chr7:25125230-25125428 | Rare:81; Clinvar:3 | ||||
| chr7:26200657-26200993 | Common:2; Rare:173 | ||||
| chr7:26201376-26201552 | Rare:63 | ||||
| chr7:26201590-26201795 | Common:2; Rare:108 | ||||
| chr7:27095974-27096167 | Rare:54 |