| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:135170623-135170986 | Common:6; Rare:121 | ||||
| chr7:135211498-135211698 | Common:2; Rare:97 | ||||
| chr7:135510084-135510352 | Common:2; Rare:62 | ||||
| chr7:135557888-135557953 | Common:1; Rare:24 | ||||
| chr7:135662318-135662548 | Common:4; Rare:98 | ||||
| chr7:135977294-135977530 | Common:2; Rare:92 | ||||
| chr7:139109343-139109427 | Common:1; Rare:28 | ||||
| chr7:139133705-139133809 | Rare:26 | ||||
| chr7:139340345-139340494 | Common:1; Rare:37 | ||||
| chr7:139341241-139341375 | Rare:28 | ||||
| chr7:139359677-139360010 | Common:3; Rare:130 | ||||
| chr7:140696607-140696749 | Common:1; Rare:51 | ||||
| chr7:141014920-141015123 | Rare:45 | ||||
| chr7:141551271-141551434 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141737988-141738464 | Common:4; Rare:141 |