| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58554945-58555344 | Common:2; Rare:131 | ||||
| chr19:58573517-58573587 | Common:1; Rare:19 | ||||
| chr2:677346-677552 | Common:1; Rare:90 | ||||
| chr2:1744389-1744604 | Common:1; Rare:78 | ||||
| chr2:3377796-3377953 | Rare:41 | ||||
| chr2:3379625-3379787 | Common:2; Rare:67 | ||||
| chr2:3519478-3519660 | Common:2; Rare:57 | ||||
| chr2:3558269-3558565 | Common:6; Rare:108 | ||||
| chr2:3575092-3575447 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9422870-9422897 | Rare:5 | ||||
| chr2:9423098-9423700 | Common:2; Rare:159 | ||||
| chr2:9474476-9474642 | Common:7; Rare:73 | ||||
| chr2:9555626-9556060 | Common:3; Rare:143 | ||||
| chr2:9630946-9631346 | Common:3; Rare:128 | ||||
| chr2:9843405-9843539 | Common:3; Rare:37 |