| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:156640506-156640685 | Common:4; Rare:96 | ||||
| chr7:156893210-156893409 | Common:2; Rare:72 | ||||
| chr7:157138617-157138942 | Common:4; Rare:90 | ||||
| chr7:157336769-157337093 | Common:3; Rare:157; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704737-158704955 | Common:1; Rare:76 | ||||
| chr7:158856419-158856707 | Common:7; Rare:102 | ||||
| chr8:232180-232470 | Common:3; Rare:121 | ||||
| chr8:233024-233081 | Rare:15 | ||||
| chr8:406822-407018 | Rare:78 | ||||
| chr8:731159-731444 | Common:3; Rare:112 | ||||
| chr8:2127579-2127800 | Common:7; Rare:39 | ||||
| chr8:6406521-6406670 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708165-6708386 | Common:3; Rare:95 | ||||
| chr8:6708494-6708822 | Common:2; Rare:147 | ||||
| chr8:6835501-6835561 | Rare:30 |