| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139109303-139109439 | Common:1; Rare:42 | ||||
| chr7:139109712-139109851 | Common:1; Rare:33 | ||||
| chr7:139341257-139341380 | Rare:29 | ||||
| chr7:139359426-139359528 | Rare:40 | ||||
| chr7:139359682-139360008 | Common:3; Rare:127 | ||||
| chr7:139483655-139483816 | Common:2; Rare:56 | ||||
| chr7:139777610-139777802 | Common:1; Rare:45 | ||||
| chr7:139778188-139778511 | Common:4; Rare:69 | ||||
| chr7:139778709-139778768 | Rare:18 | ||||
| chr7:140177033-140177329 | Common:2; Rare:109 | ||||
| chr7:140479179-140479235 | Rare:19 | ||||
| chr7:140696642-140696735 | Common:1; Rare:29 | ||||
| chr7:141014618-141014744 | Rare:21 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738587 | Common:4; Rare:159 |