| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:32728737-32728869 | Common:7; Rare:48 | ||||
| chr7:32942468-32942639 | Common:1; Rare:45 | ||||
| chr7:38335581-38335804 | Common:2; Rare:49 | ||||
| chr7:40763086-40763388 | Common:3; Rare:50 | ||||
| chr7:40900047-40900268 | Common:4; Rare:52 | ||||
| chr7:41705406-41705614 | Common:1; Rare:44 | ||||
| chr7:41705661-41705751 | Rare:9 | ||||
| chr7:43645249-43645528 | Common:1; Rare:66 | ||||
| chr7:44038979-44039221 | Common:5; Rare:40 | ||||
| chr7:44107910-44108103 | Common:2; Rare:63; Clinvar (pathogenic):1 | ||||
| chr7:44467589-44467882 | Common:3; Rare:58 | ||||
| chr7:44884162-44884438 | Common:1; Rare:66 | ||||
| chr7:45192593-45192683 | Common:1; Rare:15 | ||||
| chr7:45768893-45769141 | Common:3; Rare:71 | ||||
| chr7:64463722-64463861 | Common:1; Rare:36 |