| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71663800-71664042 | Common:1; Rare:74 | ||||
| chr12:74537743-74538011 | Common:1; Rare:92 | ||||
| chr12:75390891-75391109 | Common:1; Rare:69 | ||||
| chr12:75511578-75511851 | Rare:80 | ||||
| chr12:76764040-76764281 | Common:2; Rare:101 | ||||
| chr12:76878983-76879216 | Rare:81 | ||||
| chr12:79934907-79935355 | Common:1; Rare:175 | ||||
| chr12:80707197-80707722 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr12:80716777-80716975 | Common:1; Rare:43 | ||||
| chr12:80937688-80937843 | Common:1; Rare:49 | ||||
| chr12:82358377-82358555 | Rare:73 | ||||
| chr12:82358736-82358899 | Common:3; Rare:85 | ||||
| chr12:88142066-88142394 | Rare:91; Clinvar:3 | ||||
| chr12:88580440-88580550 | Common:1; Rare:39 | ||||
| chr12:89352473-89352716 | Rare:75 |