| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151232382-151232578 | Common:1; Rare:116 | ||||
| chr7:151248637-151248749 | Common:1; Rare:23 | ||||
| chr7:151341524-151341866 | Common:8; Rare:203 | ||||
| chr7:151519891-151520081 | Common:1; Rare:57 | ||||
| chr7:151520087-151520265 | Common:1; Rare:37 | ||||
| chr7:151876880-151877640 | Common:5; Rare:234; Clinvar:7; Clinvar (benign):1 | ||||
| chr7:152025561-152025827 | Common:2; Rare:190 | ||||
| chr7:152435835-152436303 | Rare:157 | ||||
| chr7:152676038-152676330 | Common:4; Rare:237; Clinvar:1; Clinvar (benign):25; Clinvar (pathogenic):1 | ||||
| chr7:152759615-152759890 | Common:8; Rare:191 | ||||
| chr7:155002922-155003594 | Common:22; Rare:364 | ||||
| chr7:155297588-155298003 | Common:16; Rare:313 | ||||
| chr7:155298900-155299300 | Common:1; Rare:119 | ||||
| chr7:155644155-155644746 | Common:6; Rare:322 | ||||
| chr7:156640430-156640790 | Common:8; Rare:302 |