| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26864562-26864806 | Common:2; Rare:76 | ||||
| chr7:27095918-27096233 | Rare:86 | ||||
| chr7:27740061-27740192 | Common:5; Rare:34 | ||||
| chr7:28180569-28180888 | Common:4; Rare:89 | ||||
| chr7:30504773-30505090 | Common:2; Rare:102 | ||||
| chr7:30594727-30594970 | Common:3; Rare:119; Clinvar:5; Clinvar (benign):6 | ||||
| chr7:32490361-32490507 | Common:1; Rare:44 | ||||
| chr7:32495238-32495598 | Common:1; Rare:92 | ||||
| chr7:35800725-35801286 | Common:3; Rare:213 | ||||
| chr7:38178053-38178396 | Common:3; Rare:101 | ||||
| chr7:39566312-39566458 | Common:1; Rare:68 | ||||
| chr7:39623475-39623812 | Rare:107 | ||||
| chr7:40134581-40135016 | Rare:136; Clinvar:1 | ||||
| chr7:41703067-41703270 | Common:1; Rare:29 | ||||
| chr7:42932159-42932410 | Rare:102 |