| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:117520484-117520759 | Common:5; Rare:60 | ||||
| chr8:118109945-118110809 | Common:2; Rare:219; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:118111187-118111377 | Common:1; Rare:38; Clinvar (benign):2 | ||||
| chr8:119832811-119832964 | Common:2; Rare:58 | ||||
| chr8:120445072-120445518 | Common:1; Rare:125 | ||||
| chr8:120811125-120811211 | Common:3; Rare:30 | ||||
| chr8:121641035-121641304 | Common:12; Rare:41 | ||||
| chr8:121641359-121641609 | Rare:49 | ||||
| chr8:122781521-122781689 | Rare:26 | ||||
| chr8:123041970-123042564 | Common:3; Rare:164 | ||||
| chr8:123274214-123274321 | Rare:15 | ||||
| chr8:123274450-123274646 | Common:1; Rare:68 | ||||
| chr8:123396181-123396508 | Common:1; Rare:154 | ||||
| chr8:123416323-123416833 | Rare:133 | ||||
| chr8:124474148-124474332 | Common:1; Rare:37 |