| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44573891-44574053 | Common:3; Rare:45 | ||||
| chr7:44582164-44582490 | Common:1; Rare:126 | ||||
| chr7:44606459-44606635 | Common:1; Rare:60 | ||||
| chr7:44748307-44748587 | Common:2; Rare:69 | ||||
| chr7:44796397-44796789 | Common:3; Rare:151 | ||||
| chr7:45111687-45111799 | Common:1; Rare:38 | ||||
| chr7:47979521-47979726 | Rare:79 | ||||
| chr7:50450329-50450453 | Rare:51 | ||||
| chr7:55572341-55572655 | Common:1; Rare:116 | ||||
| chr7:56051439-56051864 | Common:1; Rare:164; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114768-66114904 | Common:1; Rare:67 | ||||
| chr7:66115194-66115354 | Rare:35 | ||||
| chr7:66682030-66682192 | Common:6; Rare:75 | ||||
| chr7:73683419-73683622 | Common:3; Rare:81 | ||||
| chr7:73738791-73739107 | Common:2; Rare:98 |