| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140696602-140696805 | Common:1; Rare:74 | ||||
| chr7:140697000-140697026 | Rare:3 | ||||
| chr7:140697094-140697329 | Rare:82 | ||||
| chr7:141014571-141014744 | Rare:25 | ||||
| chr7:141014920-141015106 | Rare:41 | ||||
| chr7:141073996-141074319 | Rare:81 | ||||
| chr7:141551265-141551428 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141737954-141738628 | Common:6; Rare:183 | ||||
| chr7:142854990-142855195 | Common:3; Rare:57 | ||||
| chr7:143263390-143263525 | Rare:42 | ||||
| chr7:143361359-143361490 | Rare:24 | ||||
| chr7:143361751-143361967 | Rare:57 | ||||
| chr7:143362050-143362308 | Rare:40 | ||||
| chr7:143362599-143362945 | Common:1; Rare:95 | ||||
| chr7:143380920-143381011 | Rare:26 |