| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141995694-141995928 | Common:1; Rare:44 | ||||
| chr7:142854995-142855134 | Common:2; Rare:42 | ||||
| chr7:143263671-143263859 | Rare:33 | ||||
| chr7:143288019-143288258 | Common:1; Rare:67 | ||||
| chr7:143380954-143381179 | Rare:71 | ||||
| chr7:143408814-143408960 | Rare:35 | ||||
| chr7:144355192-144355492 | Rare:2 | ||||
| chr7:144835973-144836106 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr7:148698851-148698978 | Common:1; Rare:38 | ||||
| chr7:149028334-149028573 | Common:2; Rare:91 | ||||
| chr7:149028647-149028980 | Common:1; Rare:109 | ||||
| chr7:149090657-149090915 | Rare:72 | ||||
| chr7:149126220-149126438 | Common:6; Rare:73 | ||||
| chr7:149261915-149262270 | Common:3; Rare:112 | ||||
| chr7:149873852-149874056 | Common:3; Rare:80 |