| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341196-139341397 | Rare:55 | ||||
| chr7:139359692-139359988 | Common:3; Rare:117 | ||||
| chr7:139483627-139483830 | Common:2; Rare:74 | ||||
| chr7:139777991-139778248 | Common:1; Rare:61 | ||||
| chr7:140176939-140177271 | Common:2; Rare:119 | ||||
| chr7:140351865-140352079 | Common:4; Rare:49 | ||||
| chr7:140403995-140404227 | Rare:41 | ||||
| chr7:140404280-140404438 | Common:2; Rare:21 | ||||
| chr7:140478535-140478820 | Common:5; Rare:81 | ||||
| chr7:140479243-140479458 | Common:1; Rare:73 | ||||
| chr7:140479464-140479658 | Rare:65 | ||||
| chr7:140640799-140640923 | Rare:35 | ||||
| chr7:140696602-140697049 | Common:2; Rare:140 | ||||
| chr7:140924728-140925091 | Common:2; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:141014589-141014726 | Rare:23 |