| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151877113-151877509 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152025544-152025802 | Common:1; Rare:103 | ||||
| chr7:152676135-152676276 | Common:2; Rare:50 | ||||
| chr7:155644377-155644879 | Common:6; Rare:160 | ||||
| chr7:156640546-156640685 | Common:3; Rare:72 | ||||
| chr7:157336918-157337070 | Common:1; Rare:71; Clinvar:1 | ||||
| chr7:158704764-158704975 | Common:1; Rare:75 | ||||
| chr7:158856423-158856680 | Common:6; Rare:93 | ||||
| chr8:232176-232410 | Common:3; Rare:91 | ||||
| chr8:406756-407025 | Common:2; Rare:125 | ||||
| chr8:6406527-6406670 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6877926-6878230 | Common:2; Rare:78 | ||||
| chr8:10839819-10840094 | Common:2; Rare:91 | ||||
| chr8:11802446-11802801 | Common:6; Rare:191 | ||||
| chr8:12436350-12436537 | Common:4; Rare:35 |