| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341194-139341473 | Common:1; Rare:87 | ||||
| chr7:139359656-139360042 | Common:3; Rare:151 | ||||
| chr7:139778038-139778255 | Common:1; Rare:47 | ||||
| chr7:140062537-140062626 | Rare:33 | ||||
| chr7:140176938-140177272 | Common:2; Rare:119 | ||||
| chr7:140479283-140479697 | Common:1; Rare:137 | ||||
| chr7:140696635-140696756 | Common:1; Rare:47 | ||||
| chr7:140696814-140696842 | Rare:10 | ||||
| chr7:140696944-140697049 | Rare:18 | ||||
| chr7:140697051-140697318 | Rare:87 | ||||
| chr7:141014588-141014726 | Rare:23 | ||||
| chr7:141551272-141551294 | Common:1; Rare:4; Clinvar:1 | ||||
| chr7:141551298-141551457 | Rare:53; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737894-141738639 | Common:6; Rare:196 | ||||
| chr7:143263432-143263583 | Rare:51 |