| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:155003302-155003480 | Common:5; Rare:75 | ||||
| chr7:155298974-155299213 | Rare:50 | ||||
| chr7:155644103-155644206 | Rare:39 | ||||
| chr7:155644377-155644935 | Common:6; Rare:178 | ||||
| chr7:156640529-156640800 | Common:3; Rare:129 | ||||
| chr7:156893177-156893414 | Common:3; Rare:91; Clinvar (benign):1 | ||||
| chr7:157138633-157138988 | Common:4; Rare:112 | ||||
| chr7:157336761-157337138 | Common:3; Rare:179; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704736-158705018 | Common:1; Rare:106 | ||||
| chr7:158856414-158856716 | Common:7; Rare:105 | ||||
| chr8:232093-232486 | Common:3; Rare:160 | ||||
| chr8:233024-233094 | Rare:18 | ||||
| chr8:2127530-2127836 | Common:14; Rare:77 | ||||
| chr8:4994418-4994681 | Rare:100 | ||||
| chr8:6406468-6406689 | Common:5; Rare:116; Clinvar:2; Clinvar (benign):1 |