| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:107497287-107497638 | Common:2; Rare:107 | ||||
| chr8:107497658-107498069 | Common:1; Rare:78 | ||||
| chr8:109334060-109334471 | Common:1; Rare:107 | ||||
| chr8:116874204-116874236 | Rare:11 | ||||
| chr8:118111388-118111469 | Rare:14; Clinvar:1 | ||||
| chr8:118621851-118622163 | Common:2; Rare:104 | ||||
| chr8:118951813-118952152 | Common:1; Rare:100; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:118952173-118952250 | Rare:14 | ||||
| chr8:119832815-119832920 | Common:1; Rare:40 | ||||
| chr8:120445087-120445454 | Common:1; Rare:92 | ||||
| chr8:123274225-123274342 | Rare:18 | ||||
| chr8:123396369-123396572 | Common:2; Rare:94 | ||||
| chr8:123416323-123416730 | Rare:105 | ||||
| chr8:124539037-124539280 | Common:2; Rare:121; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091618-125091933 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 |