| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140696607-140696741 | Common:1; Rare:46 | ||||
| chr7:140696817-140697049 | Common:1; Rare:60 | ||||
| chr7:141014878-141015143 | Rare:69 | ||||
| chr7:141074186-141074262 | Rare:19 | ||||
| chr7:141551165-141551434 | Common:3; Rare:66; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141737900-141738624 | Common:6; Rare:194 | ||||
| chr7:143263397-143263517 | Rare:36 | ||||
| chr7:143288276-143288451 | Common:1; Rare:70 | ||||
| chr7:143380953-143381118 | Rare:47 | ||||
| chr7:143882817-143883003 | Rare:48 | ||||
| chr7:143902109-143902304 | Common:5; Rare:61 | ||||
| chr7:144835997-144836106 | Rare:32 | ||||
| chr7:148339213-148339567 | Common:6; Rare:86 | ||||
| chr7:148698399-148698972 | Common:5; Rare:197 | ||||
| chr7:148884177-148884472 | Common:1; Rare:137; Clinvar:3; Clinvar (benign):1 |