| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359648-139360008 | Common:3; Rare:145 | ||||
| chr7:140177042-140177329 | Common:2; Rare:107 | ||||
| chr7:140479179-140479235 | Rare:19 | ||||
| chr7:140924641-140925030 | Common:3; Rare:136; Clinvar:5; Clinvar (benign):6 | ||||
| chr7:141014909-141015030 | Rare:30 | ||||
| chr7:141551322-141551428 | Rare:33; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738468 | Common:4; Rare:134 | ||||
| chr7:142854990-142855138 | Common:2; Rare:44 | ||||
| chr7:143288041-143288447 | Common:2; Rare:137 | ||||
| chr7:143620647-143620986 | Rare:14 | ||||
| chr7:143902104-143902292 | Common:5; Rare:60 | ||||
| chr7:144195590-144195858 | Rare:4 | ||||
| chr7:144355185-144355496 | Rare:2 | ||||
| chr7:144835983-144836156 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr7:148698360-148698978 | Common:6; Rare:205 |