| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44123516-44123749 | Common:4; Rare:66 | ||||
| chr7:44573873-44574063 | Common:3; Rare:58 | ||||
| chr7:44582169-44582435 | Common:1; Rare:91 | ||||
| chr7:44606459-44606641 | Common:1; Rare:61 | ||||
| chr7:44606776-44607055 | Common:2; Rare:88 | ||||
| chr7:44748327-44748591 | Common:2; Rare:63 | ||||
| chr7:44796390-44796790 | Common:3; Rare:154 | ||||
| chr7:44999986-45000261 | Common:1; Rare:65 | ||||
| chr7:45111665-45111818 | Common:1; Rare:58 | ||||
| chr7:45921269-45921411 | Rare:37 | ||||
| chr7:48088915-48089269 | Common:6; Rare:94 | ||||
| chr7:50450322-50450447 | Common:1; Rare:52 | ||||
| chr7:55018895-55019274 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:55365935-55366101 | Rare:71 | ||||
| chr7:55572309-55572561 | Common:1; Rare:102 |