| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76053089-76053360 | Common:1; Rare:72 | ||||
| chr12:76083856-76084085 | Rare:60 | ||||
| chr12:76084555-76084799 | Common:1; Rare:79 | ||||
| chr12:76348349-76348578 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559511-76559929 | Common:2; Rare:139 | ||||
| chr12:76763872-76764302 | Common:5; Rare:182 | ||||
| chr12:76878954-76879145 | Rare:67 | ||||
| chr12:79690403-79690672 | Common:1; Rare:77 | ||||
| chr12:79690965-79691221 | Common:1; Rare:85 | ||||
| chr12:79934713-79935406 | Common:1; Rare:235 | ||||
| chr12:80937670-80937859 | Common:1; Rare:58 | ||||
| chr12:81077710-81078143 | Rare:90 | ||||
| chr12:82358264-82358556 | Common:1; Rare:141 | ||||
| chr12:82358727-82358896 | Common:3; Rare:89 | ||||
| chr12:82686715-82686915 | Rare:65 |