| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134986450-134986561 | Common:3; Rare:48 | ||||
| chr7:135147737-135148129 | Common:1; Rare:82 | ||||
| chr7:135170656-135170973 | Common:5; Rare:103 | ||||
| chr7:135211476-135211791 | Common:2; Rare:145 | ||||
| chr7:135662357-135662520 | Common:4; Rare:69 | ||||
| chr7:139109327-139109487 | Common:1; Rare:48 | ||||
| chr7:139109696-139109840 | Common:1; Rare:34 | ||||
| chr7:139133677-139133792 | Rare:25 | ||||
| chr7:139341197-139341369 | Rare:39 | ||||
| chr7:139359672-139359988 | Common:3; Rare:125 | ||||
| chr7:140027333-140027503 | Common:1; Rare:43 | ||||
| chr7:140177033-140177329 | Common:2; Rare:109 | ||||
| chr7:140479313-140479678 | Common:1; Rare:112 | ||||
| chr7:141551342-141551423 | Rare:23; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738228-141738464 | Rare:93 |