| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:74537678-74537955 | Common:1; Rare:91 | ||||
| chr12:75334379-75334779 | Common:1; Rare:144 | ||||
| chr12:75390893-75391103 | Common:1; Rare:62 | ||||
| chr12:75511460-75511920 | Rare:133 | ||||
| chr12:76031573-76031896 | Common:1; Rare:102 | ||||
| chr12:76083857-76084078 | Rare:60 | ||||
| chr12:76084642-76084864 | Common:1; Rare:72 | ||||
| chr12:76347750-76348240 | Common:1; Rare:126; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr12:76348349-76348605 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76558837-76559455 | Common:5; Rare:142 | ||||
| chr12:76559680-76559991 | Rare:111 | ||||
| chr12:76763930-76764336 | Common:4; Rare:171 | ||||
| chr12:76764360-76764620 | Rare:72 | ||||
| chr12:76878862-76879285 | Rare:130 | ||||
| chr12:77065513-77065808 | Common:2; Rare:94 |