| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:135211503-135211729 | Common:2; Rare:106 | ||||
| chr7:135510074-135510277 | Common:2; Rare:43 | ||||
| chr7:135662370-135662511 | Common:3; Rare:59 | ||||
| chr7:135977303-135977530 | Common:2; Rare:88 | ||||
| chr7:139109310-139109650 | Common:1; Rare:96 | ||||
| chr7:139109693-139109835 | Common:1; Rare:33 | ||||
| chr7:139341166-139341369 | Rare:46 | ||||
| chr7:139359682-139359982 | Common:3; Rare:120 | ||||
| chr7:140674409-140674496 | Common:1; Rare:16 | ||||
| chr7:140696602-140696735 | Common:1; Rare:42 | ||||
| chr7:141014904-141015120 | Rare:50 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738027-141738470 | Common:4; Rare:134 | ||||
| chr7:142771311-142771469 | Common:2; Rare:13 | ||||
| chr7:143263383-143263509 | Rare:35 |