| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:135977304-135977563 | Common:3; Rare:97 | ||||
| chr7:138002013-138002162 | Common:1; Rare:39 | ||||
| chr7:139109337-139109427 | Common:1; Rare:29 | ||||
| chr7:139133675-139133849 | Rare:47 | ||||
| chr7:139231016-139231265 | Common:2; Rare:87 | ||||
| chr7:139341241-139341375 | Rare:28 | ||||
| chr7:139359692-139359982 | Common:3; Rare:115 | ||||
| chr7:139360049-139360317 | Common:1; Rare:104 | ||||
| chr7:140696597-140696735 | Common:1; Rare:43 | ||||
| chr7:141551090-141551434 | Common:3; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738033-141738464 | Common:4; Rare:132 | ||||
| chr7:142854990-142855133 | Common:2; Rare:42 | ||||
| chr7:143380886-143381362 | Common:2; Rare:144 | ||||
| chr7:143382083-143382306 | Common:1; Rare:66 | ||||
| chr7:143407707-143407815 | Common:1; Rare:12 |