| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:136868457-136868689 | Common:1; Rare:40 | ||||
| chr7:137343470-137343800 | Rare:111 | ||||
| chr7:139133654-139133834 | Rare:46 | ||||
| chr7:139341234-139341369 | Rare:28 | ||||
| chr7:139359648-139359982 | Common:3; Rare:138 | ||||
| chr7:139360178-139360218 | Rare:14 | ||||
| chr7:140696607-140696741 | Common:1; Rare:46 | ||||
| chr7:141551265-141551428 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738021-141738464 | Common:4; Rare:134 | ||||
| chr7:143362070-143362293 | Rare:35 | ||||
| chr7:143882817-143882964 | Rare:39 | ||||
| chr7:144836022-144836156 | Common:1; Rare:46 | ||||
| chr7:148698446-148698657 | Common:4; Rare:67 | ||||
| chr7:149090672-149090876 | Rare:57 | ||||
| chr7:149126242-149126432 | Common:6; Rare:63 |