| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140478509-140478627 | Common:5; Rare:28 | ||||
| chr7:140478758-140479096 | Common:5; Rare:106 | ||||
| chr7:140479169-140479259 | Common:1; Rare:30 | ||||
| chr7:140479301-140479644 | Common:1; Rare:108 | ||||
| chr7:140696602-140696759 | Common:1; Rare:59 | ||||
| chr7:140696937-140697026 | Rare:16 | ||||
| chr7:140697087-140697236 | Rare:43 | ||||
| chr7:140924187-140924241 | Rare:10 | ||||
| chr7:140924655-140925114 | Common:3; Rare:178; Clinvar:4; Clinvar (benign):6 | ||||
| chr7:140925168-140925207 | Rare:7 | ||||
| chr7:141014464-141014517 | Common:1; Rare:14 | ||||
| chr7:141014604-141014820 | Rare:34 | ||||
| chr7:141014924-141015143 | Rare:54 | ||||
| chr7:141551246-141551434 | Common:2; Rare:52; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738183-141738647 | Common:2; Rare:139 |