| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501986-21502109 | Common:2; Rare:30 | ||||
| chr12:21502229-21502336 | Rare:21 | ||||
| chr12:21527774-21527976 | Common:1; Rare:66 | ||||
| chr12:21656813-21656997 | Common:3; Rare:33 | ||||
| chr12:21657000-21657080 | Common:1; Rare:18 | ||||
| chr12:21657291-21657504 | Rare:54 | ||||
| chr12:21657621-21658062 | Common:5; Rare:131; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21757820-21757936 | Common:1; Rare:19 | ||||
| chr12:21774394-21774627 | Rare:63; Clinvar (benign):1 | ||||
| chr12:21774673-21775245 | Rare:105 | ||||
| chr12:21940609-21940778 | Rare:33 | ||||
| chr12:21941016-21941091 | Rare:20 | ||||
| chr12:21941280-21941453 | Rare:44 | ||||
| chr12:21941631-21941730 | Rare:19 | ||||
| chr12:21941818-21942337 | Common:5; Rare:106 |