| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134646577-134646867 | Common:6; Rare:86 | ||||
| chr7:134779477-134779740 | Rare:48 | ||||
| chr7:135148009-135148129 | Rare:32 | ||||
| chr7:135170486-135170816 | Common:3; Rare:119 | ||||
| chr7:136868464-136868864 | Common:2; Rare:83 | ||||
| chr7:139341272-139341386 | Rare:30 | ||||
| chr7:139359692-139360015 | Common:3; Rare:123 | ||||
| chr7:140177042-140177309 | Common:2; Rare:101 | ||||
| chr7:141014623-141014766 | Rare:24 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738066-141738544 | Common:4; Rare:145 | ||||
| chr7:142854997-142855126 | Common:2; Rare:39 | ||||
| chr7:143263392-143263532 | Rare:45 | ||||
| chr7:144836026-144836106 | Rare:26 | ||||
| chr7:149090705-149090870 | Rare:44 |