| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:131327777-131327897 | Rare:43 | ||||
| chr7:134527453-134527839 | Common:2; Rare:65 | ||||
| chr7:134646582-134646904 | Common:7; Rare:103 | ||||
| chr7:134986330-134986556 | Common:5; Rare:80 | ||||
| chr7:135147985-135148109 | Rare:27 | ||||
| chr7:135170640-135170826 | Common:2; Rare:71 | ||||
| chr7:139109337-139109449 | Common:1; Rare:35 | ||||
| chr7:139109718-139109821 | Common:1; Rare:27 | ||||
| chr7:139359672-139360008 | Common:3; Rare:130 | ||||
| chr7:141014628-141014767 | Rare:23 | ||||
| chr7:141551322-141551423 | Rare:32; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738468 | Common:4; Rare:132 | ||||
| chr7:142854990-142855190 | Common:3; Rare:57 | ||||
| chr7:143288150-143288433 | Common:1; Rare:101 | ||||
| chr7:143380931-143381097 | Rare:47 |