| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14803393-14803691 | Common:3; Rare:83 | ||||
| chr12:14814180-14814377 | Common:1; Rare:26 | ||||
| chr12:14884466-14884611 | Rare:24 | ||||
| chr12:14885714-14885980 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:14961538-14961729 | Common:2; Rare:51 | ||||
| chr12:15221244-15221586 | Common:1; Rare:100 | ||||
| chr12:15789267-15789641 | Common:1; Rare:125 | ||||
| chr12:15882254-15882816 | Common:1; Rare:186 | ||||
| chr12:16606465-16606798 | Rare:71 | ||||
| chr12:18261401-18261573 | Common:1; Rare:37 | ||||
| chr12:19129425-19129825 | Common:3; Rare:167 | ||||
| chr12:19439337-19439697 | Common:3; Rare:132 | ||||
| chr12:19439805-19439954 | Common:1; Rare:76 | ||||
| chr12:19440170-19440370 | Rare:61 | ||||
| chr12:19440578-19440664 | Common:1; Rare:26 |