| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141074035-141074319 | Rare:67 | ||||
| chr7:141551306-141551467 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141701330-141701750 | Common:3; Rare:79 | ||||
| chr7:141702097-141702268 | Common:2; Rare:52 | ||||
| chr7:141738171-141738451 | Rare:105 | ||||
| chr7:143263384-143263514 | Rare:36 | ||||
| chr7:143287986-143288464 | Common:2; Rare:154 | ||||
| chr7:143288545-143289357 | Common:5; Rare:204 | ||||
| chr7:143381167-143381372 | Common:1; Rare:69 | ||||
| chr7:143882825-143883019 | Rare:48 | ||||
| chr7:143885227-143885627 | Common:2; Rare:175 | ||||
| chr7:143902114-143902321 | Common:5; Rare:62 | ||||
| chr7:144835864-144836203 | Common:3; Rare:120; Clinvar (benign):2 | ||||
| chr7:148698366-148698470 | Common:1; Rare:29 | ||||
| chr7:148698712-148698960 | Common:1; Rare:89 |