| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139231184-139231276 | Common:1; Rare:42 | ||||
| chr7:139341241-139341379 | Rare:32 | ||||
| chr7:139341711-139341824 | Common:4; Rare:29 | ||||
| chr7:139359667-139360024 | Common:3; Rare:136 | ||||
| chr7:139777708-139778075 | Common:2; Rare:98 | ||||
| chr7:139778185-139778389 | Common:3; Rare:51 | ||||
| chr7:140177030-140177349 | Common:2; Rare:118 | ||||
| chr7:140398453-140398579 | Common:1; Rare:44 | ||||
| chr7:140479316-140479551 | Rare:73 | ||||
| chr7:140696597-140696799 | Common:1; Rare:74 | ||||
| chr7:140696904-140697002 | Common:1; Rare:19 | ||||
| chr7:140924684-140925092 | Common:3; Rare:148; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:141014617-141015093 | Rare:107 | ||||
| chr7:141551322-141551441 | Rare:35; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738033-141738628 | Common:5; Rare:165 |