| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:17298454-17298659 | Common:3; Rare:49 | ||||
| chr7:17940412-17940613 | Common:2; Rare:103 | ||||
| chr7:18086685-18086999 | Common:4; Rare:127 | ||||
| chr7:18495346-18495807 | Rare:107 | ||||
| chr7:18495923-18496318 | Common:3; Rare:102 | ||||
| chr7:22822757-22822969 | Common:3; Rare:78 | ||||
| chr7:23105636-23105923 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23106073-23106213 | Rare:35 | ||||
| chr7:23181824-23182128 | Common:2; Rare:121 | ||||
| chr7:23299193-23299431 | Common:2; Rare:124 | ||||
| chr7:23467909-23468071 | Common:1; Rare:40 | ||||
| chr7:23470326-23470573 | Rare:76 | ||||
| chr7:23531948-23532130 | Common:2; Rare:74 | ||||
| chr7:23597226-23597437 | Rare:72 | ||||
| chr7:23680029-23680215 | Common:5; Rare:55 |