| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151080793-151080962 | Rare:51 | ||||
| chr7:152025569-152025775 | Rare:83 | ||||
| chr7:152676101-152676280 | Common:2; Rare:69; Clinvar (benign):6 | ||||
| chr7:155644377-155644724 | Common:2; Rare:120 | ||||
| chr7:156640554-156640685 | Common:2; Rare:68 | ||||
| chr7:157336749-157337081 | Common:2; Rare:159; Clinvar:2 | ||||
| chr7:158856362-158856680 | Common:7; Rare:109 | ||||
| chr8:232180-232465 | Common:3; Rare:118 | ||||
| chr8:6406557-6406680 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:9151537-9151722 | Common:1; Rare:60 | ||||
| chr8:10839824-10840126 | Common:3; Rare:100 | ||||
| chr8:11802419-11802799 | Common:6; Rare:213 | ||||
| chr8:13566760-13566920 | Common:6; Rare:61 | ||||
| chr8:17246591-17247027 | Common:5; Rare:188 | ||||
| chr8:17922616-17922911 | Common:4; Rare:110 |