| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71754702-71754913 | Common:3; Rare:56 | ||||
| chr12:71755130-71755237 | Common:5; Rare:26 | ||||
| chr12:71839667-71839807 | Common:1; Rare:57 | ||||
| chr12:74537704-74537938 | Common:1; Rare:80 | ||||
| chr12:75390876-75391109 | Common:1; Rare:70 | ||||
| chr12:75480663-75480891 | Rare:50 | ||||
| chr12:76031491-76031814 | Common:1; Rare:113 | ||||
| chr12:76053086-76053376 | Common:1; Rare:80 | ||||
| chr12:76083912-76084076 | Rare:49 | ||||
| chr12:76084555-76084793 | Common:1; Rare:77 | ||||
| chr12:76085035-76085085 | Common:1; Rare:12 | ||||
| chr12:76348360-76348502 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559696-76559880 | Rare:73 | ||||
| chr12:76764017-76764269 | Common:2; Rare:102 | ||||
| chr12:76879000-76879216 | Rare:67 |