| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128409932-128410260 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455739-128455903 | Common:2; Rare:92 | ||||
| chr7:129054861-129055226 | Common:2; Rare:71 | ||||
| chr7:129611613-129611811 | Common:1; Rare:62 | ||||
| chr7:131109892-131110129 | Common:1; Rare:42 | ||||
| chr7:131327681-131327927 | Rare:80 | ||||
| chr7:134448778-134448902 | Common:1; Rare:15 | ||||
| chr7:134646582-134646856 | Common:6; Rare:77 | ||||
| chr7:134779261-134779748 | Rare:78 | ||||
| chr7:135170438-135170849 | Common:3; Rare:145 | ||||
| chr7:135211503-135211725 | Common:2; Rare:105 | ||||
| chr7:135977033-135977195 | Rare:48 | ||||
| chr7:136868585-136868799 | Common:1; Rare:48 | ||||
| chr7:136868809-136869306 | Common:3; Rare:91; Clinvar (benign):3 | ||||
| chr7:139036022-139036230 | Rare:55 |