| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139036022-139036145 | Rare:34 | ||||
| chr7:139109327-139109461 | Common:1; Rare:40 | ||||
| chr7:139109712-139109727 | Common:1; Rare:3 | ||||
| chr7:139133654-139133806 | Rare:33 | ||||
| chr7:139340386-139340495 | Rare:29 | ||||
| chr7:139341245-139341379 | Rare:30 | ||||
| chr7:139359239-139359566 | Common:1; Rare:109 | ||||
| chr7:139359692-139360008 | Common:3; Rare:122 | ||||
| chr7:139777606-139777804 | Common:1; Rare:46 | ||||
| chr7:140177042-140177329 | Common:2; Rare:107 | ||||
| chr7:140479179-140479236 | Rare:20 | ||||
| chr7:140924680-140924825 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):4 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737932-141738617 | Common:6; Rare:187 | ||||
| chr7:142854998-142855133 | Common:2; Rare:41 |