| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75511371-75511930 | Common:2; Rare:279 | ||||
| chr12:76031411-76032028 | Common:3; Rare:422 | ||||
| chr12:76032013-76032413 | Common:1; Rare:129 | ||||
| chr12:76083870-76084142 | Rare:192 | ||||
| chr12:76084536-76085116 | Common:13; Rare:401 | ||||
| chr12:76348308-76348657 | Common:5; Rare:267; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:76559487-76560040 | Common:6; Rare:441 | ||||
| chr12:76763801-76764393 | Common:18; Rare:571 | ||||
| chr12:76764426-76764601 | Rare:90 | ||||
| chr12:76878898-76879353 | Rare:240 | ||||
| chr12:77065426-77065954 | Common:8; Rare:429 | ||||
| chr12:77065960-77066149 | Rare:73 | ||||
| chr12:78863740-78864190 | Common:1; Rare:78 | ||||
| chr12:78977387-78977787 | Common:2; Rare:155 | ||||
| chr12:79044950-79045396 | Common:11; Rare:235 |