| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359456-139359528 | Rare:23 | ||||
| chr7:139359672-139360008 | Common:3; Rare:130 | ||||
| chr7:140177033-140177355 | Common:2; Rare:118 | ||||
| chr7:140479183-140479242 | Rare:21 | ||||
| chr7:140641458-140641519 | Rare:7 | ||||
| chr7:141014628-141014722 | Rare:17 | ||||
| chr7:141014920-141015015 | Rare:23 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738228-141738489 | Rare:98 | ||||
| chr7:142854990-142855138 | Common:2; Rare:44 | ||||
| chr7:143263375-143263516 | Rare:39 | ||||
| chr7:143288078-143288451 | Common:2; Rare:125 | ||||
| chr7:143380901-143381395 | Common:1; Rare:155 | ||||
| chr7:143382245-143382979 | Common:2; Rare:268 | ||||
| chr7:143902093-143902302 | Common:7; Rare:67 |