| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:109334051-109334465 | Common:1; Rare:112 | ||||
| chr8:116873974-116874228 | Common:2; Rare:86 | ||||
| chr8:116874606-116874946 | Common:6; Rare:142; Clinvar (benign):1 | ||||
| chr8:118110097-118110342 | Rare:57 | ||||
| chr8:118621818-118622163 | Common:2; Rare:111 | ||||
| chr8:118951817-118951996 | Rare:51; Clinvar:1 | ||||
| chr8:118952003-118952306 | Common:1; Rare:76; Clinvar:6; Clinvar (benign):1 | ||||
| chr8:119832815-119832916 | Common:1; Rare:38 | ||||
| chr8:120445102-120445454 | Common:1; Rare:87 | ||||
| chr8:123275358-123275533 | Rare:37 | ||||
| chr8:123396359-123396569 | Common:2; Rare:97 | ||||
| chr8:123416323-123416731 | Rare:106 | ||||
| chr8:123768501-123768544 | Rare:12 | ||||
| chr8:124539032-124539280 | Common:2; Rare:123; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091621-125091919 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):4 |