| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107318891-107319378 | Common:3; Rare:212 | ||||
| chr12:107685612-107685894 | Common:2; Rare:93 | ||||
| chr12:107761067-107761382 | Common:6; Rare:115 | ||||
| chr12:108515000-108515291 | Common:1; Rare:87 | ||||
| chr12:108561128-108561533 | Common:4; Rare:104 | ||||
| chr12:108562340-108562649 | Common:6; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:108730240-108730630 | Common:2; Rare:92 | ||||
| chr12:108731505-108731750 | Common:3; Rare:88 | ||||
| chr12:108731956-108732223 | Common:2; Rare:75 | ||||
| chr12:108857578-108857771 | Rare:95 | ||||
| chr12:109052360-109052650 | Common:3; Rare:77 | ||||
| chr12:109093425-109093630 | Common:2; Rare:75 | ||||
| chr12:109097442-109097597 | Rare:56 | ||||
| chr12:109097850-109098250 | Common:5; Rare:125 | ||||
| chr12:109154554-109154692 | Common:1; Rare:36 |