| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127651863-127652227 | Common:2; Rare:107 | ||||
| chr7:128409961-128410262 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chr7:129054889-129055239 | Common:2; Rare:66 | ||||
| chr7:129611623-129611781 | Common:1; Rare:51 | ||||
| chr7:130051340-130051443 | Rare:42 | ||||
| chr7:130205391-130205511 | Rare:53 | ||||
| chr7:131327777-131327894 | Rare:42 | ||||
| chr7:134646574-134646856 | Common:6; Rare:79 | ||||
| chr7:134779367-134779680 | Rare:50 | ||||
| chr7:135170640-135170850 | Common:2; Rare:78 | ||||
| chr7:135510074-135510331 | Common:2; Rare:58 | ||||
| chr7:135662383-135662546 | Common:3; Rare:77 | ||||
| chr7:139341206-139341369 | Rare:37 | ||||
| chr7:139359682-139359982 | Common:3; Rare:120 | ||||
| chr7:144836022-144836123 | Rare:30 |