| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134646592-134646856 | Common:5; Rare:75 | ||||
| chr7:134779548-134779735 | Rare:36 | ||||
| chr7:135170665-135170850 | Common:2; Rare:71 | ||||
| chr7:135211481-135211816 | Common:2; Rare:147 | ||||
| chr7:135662380-135662543 | Common:3; Rare:76 | ||||
| chr7:135977303-135977534 | Common:3; Rare:88 | ||||
| chr7:139109337-139109526 | Common:1; Rare:56 | ||||
| chr7:139133675-139133828 | Rare:40 | ||||
| chr7:139341245-139341369 | Rare:24 | ||||
| chr7:139359682-139359988 | Common:3; Rare:122 | ||||
| chr7:141551279-141551434 | Common:1; Rare:45; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738033-141738587 | Common:4; Rare:157 | ||||
| chr7:143407649-143407814 | Common:1; Rare:30 | ||||
| chr7:143408821-143408978 | Rare:33 | ||||
| chr7:143902122-143902298 | Common:5; Rare:56 |