| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:24914812-24915067 | Rare:60 | ||||
| chr8:24955470-24956339 | Common:1; Rare:283; Clinvar:20; Clinvar (benign):15; Clinvar (pathogenic):6 | ||||
| chr8:24956341-24956724 | Common:2; Rare:112; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:26291392-26291822 | Common:3; Rare:148 | ||||
| chr8:26382912-26383143 | Common:3; Rare:101 | ||||
| chr8:26383281-26383429 | Rare:39 | ||||
| chr8:26390238-26390450 | Common:1; Rare:38 | ||||
| chr8:26512918-26513046 | Common:1; Rare:26 | ||||
| chr8:26513815-26514301 | Common:3; Rare:107 | ||||
| chr8:26514310-26514580 | Common:1; Rare:67 | ||||
| chr8:26578187-26578418 | Rare:61 | ||||
| chr8:26867276-26867540 | Common:12; Rare:77 | ||||
| chr8:27258352-27258539 | Rare:34 | ||||
| chr8:27258579-27258622 | Rare:3 | ||||
| chr8:27311226-27311509 | Common:7; Rare:110 |