| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6970612-6970961 | Common:3; Rare:109 | ||||
| chr12:7018461-7018584 | Common:1; Rare:32 | ||||
| chr12:7092398-7092621 | Rare:49 | ||||
| chr12:7108481-7108665 | Common:1; Rare:55 | ||||
| chr12:7109144-7109365 | Rare:70 | ||||
| chr12:7189551-7189723 | Rare:64; Clinvar:4 | ||||
| chr12:8032565-8032738 | Common:4; Rare:60 | ||||
| chr12:9869347-9869649 | Common:3; Rare:47 | ||||
| chr12:10172090-10172261 | Rare:44 | ||||
| chr12:10613508-10613694 | Common:1; Rare:73 | ||||
| chr12:11171534-11171728 | Common:2; Rare:63 | ||||
| chr12:12356999-12357165 | Common:4; Rare:91 | ||||
| chr12:12611786-12612048 | Common:2; Rare:74 | ||||
| chr12:12717219-12717496 | Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725625-12725959 | Common:4; Rare:77 |