| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606776-44607078 | Common:2; Rare:98 | ||||
| chr7:44748343-44748587 | Common:2; Rare:61 | ||||
| chr7:44796388-44796793 | Common:3; Rare:155 | ||||
| chr7:44796976-44797247 | Common:1; Rare:81 | ||||
| chr7:44797964-44798064 | Rare:23 | ||||
| chr7:44884875-44885029 | Common:2; Rare:45 | ||||
| chr7:44999991-45000269 | Common:1; Rare:66 | ||||
| chr7:45111665-45111799 | Common:1; Rare:50 | ||||
| chr7:47979469-47979747 | Rare:107 | ||||
| chr7:50450306-50450466 | Common:1; Rare:70 | ||||
| chr7:51316629-51316968 | Common:4; Rare:110 | ||||
| chr7:55018920-55019295 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:55019320-55019350 | Rare:12 | ||||
| chr7:55365728-55366073 | Common:1; Rare:135 | ||||
| chr7:55366293-55366368 | Common:1; Rare:22 |