| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:156892542-156892800 | Common:12; Rare:140 | ||||
| chr7:156893098-156893426 | Common:9; Rare:253; Clinvar:6; Clinvar (benign):4 | ||||
| chr7:156949622-156949870 | Common:3; Rare:180 | ||||
| chr7:157010614-157010869 | Common:9; Rare:168 | ||||
| chr7:157138652-157139016 | Common:5; Rare:206 | ||||
| chr7:157336876-157337015 | Rare:54 | ||||
| chr7:158704707-158705187 | Common:2; Rare:286 | ||||
| chr7:158829389-158829773 | Common:12; Rare:264 | ||||
| chr7:158856399-158856705 | Common:12; Rare:179 | ||||
| chr7:159144822-159145080 | Common:10; Rare:57 | ||||
| chr8:232160-232560 | Common:4; Rare:208 | ||||
| chr8:406756-407027 | Common:2; Rare:193 | ||||
| chr8:731159-731428 | Common:6; Rare:197 | ||||
| chr8:1755616-1755837 | Common:6; Rare:102 | ||||
| chr8:1763241-1764089 | Common:75; Rare:617; Clinvar:3; Clinvar (benign):6 |