| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:124929789-124929929 | Common:3; Rare:46 | ||||
| chr7:128791241-128791481 | Common:1; Rare:61 | ||||
| chr7:129055089-129055250 | Common:1; Rare:32 | ||||
| chr7:129611623-129611813 | Common:1; Rare:59 | ||||
| chr7:131109881-131110112 | Common:1; Rare:39 | ||||
| chr7:131327670-131327926 | Rare:83 | ||||
| chr7:134646595-134646873 | Common:5; Rare:82 | ||||
| chr7:135170432-135170836 | Common:3; Rare:144 | ||||
| chr7:135977075-135977197 | Rare:40 | ||||
| chr7:136868990-136869288 | Common:2; Rare:64; Clinvar (benign):3 | ||||
| chr7:139036006-139036225 | Rare:63 | ||||
| chr7:139133675-139133828 | Rare:40 | ||||
| chr7:140696613-140696741 | Common:1; Rare:43 | ||||
| chr7:141551342-141551437 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738464 | Common:4; Rare:132 |