| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:72954680-72954811 | Common:1; Rare:27 | ||||
| chr7:73005843-73006151 | Rare:36 | ||||
| chr7:74029365-74029639 | Rare:66 | ||||
| chr7:74034212-74034257 | Rare:5 | ||||
| chr7:74038396-74038685 | Common:2; Rare:58 | ||||
| chr7:74040142-74040611 | Common:3; Rare:78 | ||||
| chr7:74041218-74041342 | Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:74044299-74044847 | Common:1; Rare:100 | ||||
| chr7:74048657-74048664 | Rare:1 | ||||
| chr7:74049046-74049279 | Common:1; Rare:14 | ||||
| chr7:74049767-74049911 | Rare:27 | ||||
| chr7:74050350-74050431 | Rare:14 | ||||
| chr7:74050512-74050725 | Common:1; Rare:38 | ||||
| chr7:74056153-74056758 | Common:4; Rare:174; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr7:74058649-74058904 | Rare:44 |