| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:131327688-131327909 | Rare:67 | ||||
| chr7:134646582-134646856 | Common:6; Rare:77 | ||||
| chr7:135148009-135148122 | Rare:30 | ||||
| chr7:135170409-135170827 | Common:3; Rare:152 | ||||
| chr7:136868601-136868872 | Common:1; Rare:58 | ||||
| chr7:136868896-136869294 | Common:3; Rare:76; Clinvar (benign):3 | ||||
| chr7:137343454-137343665 | Rare:82 | ||||
| chr7:137454923-137455202 | Common:1; Rare:67 | ||||
| chr7:138001801-138002127 | Common:1; Rare:85 | ||||
| chr7:139341197-139341387 | Rare:48 | ||||
| chr7:139359692-139360024 | Common:3; Rare:125 | ||||
| chr7:139777606-139777671 | Common:1; Rare:17 | ||||
| chr7:140177044-140177338 | Common:2; Rare:110 | ||||
| chr7:141014621-141014744 | Rare:19 | ||||
| chr7:141551294-141551434 | Rare:42; Clinvar:4; Clinvar (benign):2 |