| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152676128-152676276 | Common:2; Rare:51 | ||||
| chr7:155644172-155644225 | Rare:12 | ||||
| chr7:155644348-155644910 | Common:6; Rare:182 | ||||
| chr7:156640496-156640816 | Common:5; Rare:150 | ||||
| chr7:156893171-156893409 | Common:3; Rare:91; Clinvar (benign):1 | ||||
| chr7:157010632-157010920 | Common:5; Rare:89 | ||||
| chr7:157336904-157337085 | Common:1; Rare:84; Clinvar:2 | ||||
| chr7:158704729-158704975 | Common:1; Rare:85 | ||||
| chr7:158856423-158856750 | Common:7; Rare:116 | ||||
| chr8:232170-232486 | Common:3; Rare:135 | ||||
| chr8:233037-233082 | Rare:10 | ||||
| chr8:2127584-2127804 | Common:7; Rare:40 | ||||
| chr8:6406527-6406685 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563225-6563249 | Rare:5 | ||||
| chr8:6708165-6708370 | Common:3; Rare:81 |