| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44108670-44108983 | Common:4; Rare:71 | ||||
| chr7:44109087-44109340 | Common:1; Rare:80 | ||||
| chr7:44109974-44110352 | Common:3; Rare:146 | ||||
| chr7:44573887-44574077 | Common:3; Rare:60 | ||||
| chr7:44582129-44582474 | Common:1; Rare:132 | ||||
| chr7:44606459-44606631 | Common:1; Rare:59 | ||||
| chr7:44606812-44607052 | Common:2; Rare:68 | ||||
| chr7:44748315-44748587 | Common:2; Rare:67 | ||||
| chr7:44796388-44796784 | Common:3; Rare:153 | ||||
| chr7:44978951-44979223 | Rare:55 | ||||
| chr7:45111669-45111793 | Common:1; Rare:49 | ||||
| chr7:48089064-48089316 | Common:3; Rare:74 | ||||
| chr7:55572320-55572568 | Common:1; Rare:98 | ||||
| chr7:56051422-56051878 | Common:1; Rare:174; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:64563018-64563241 | Common:3; Rare:59 |