| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:91880657-91880822 | Common:2; Rare:47 | ||||
| chr7:91940702-91940993 | Common:5; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92134288-92134604 | Rare:101 | ||||
| chr7:92134717-92134923 | Common:3; Rare:61 | ||||
| chr7:92245675-92245986 | Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246036-92246361 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:92528288-92528881 | Common:5; Rare:189; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590025-92590123 | Rare:38 | ||||
| chr7:92833839-92834089 | Rare:56 | ||||
| chr7:92834143-92834238 | Common:1; Rare:14 | ||||
| chr7:92835131-92835421 | Common:2; Rare:72 | ||||
| chr7:92835452-92835688 | Common:1; Rare:56 | ||||
| chr7:92836355-92836626 | Rare:55 | ||||
| chr7:93148760-93148914 | Common:1; Rare:30 | ||||
| chr7:93232173-93232417 | Common:2; Rare:55 |