| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73557066-73557261 | Common:1; Rare:62 | ||||
| chr7:73557485-73557805 | Common:2; Rare:104 | ||||
| chr7:73570973-73571228 | Rare:61 | ||||
| chr7:73578547-73578918 | Common:14; Rare:106 | ||||
| chr7:73683394-73683667 | Common:3; Rare:125 | ||||
| chr7:73738739-73739047 | Common:1; Rare:104 | ||||
| chr7:74174008-74174414 | Common:2; Rare:177 | ||||
| chr7:74254271-74254517 | Rare:111 | ||||
| chr7:74289284-74289423 | Common:3; Rare:48 | ||||
| chr7:74380100-74380218 | Rare:16 | ||||
| chr7:74453713-74454037 | Common:1; Rare:84 | ||||
| chr7:75073801-75073892 | Common:2; Rare:29 | ||||
| chr7:75878826-75879087 | Common:12; Rare:92 | ||||
| chr7:75882182-75882632 | Common:2; Rare:111 | ||||
| chr7:75914930-75915168 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 |