| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:74537701-74537985 | Common:1; Rare:98 | ||||
| chr12:75390869-75391236 | Common:1; Rare:130 | ||||
| chr12:76031491-76031844 | Common:1; Rare:116 | ||||
| chr12:76084565-76084849 | Common:1; Rare:91 | ||||
| chr12:76348345-76348498 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559696-76559902 | Rare:78 | ||||
| chr12:76763923-76764279 | Common:4; Rare:149 | ||||
| chr12:76844895-76845078 | Common:1; Rare:33 | ||||
| chr12:76878948-76879106 | Rare:51 | ||||
| chr12:77065523-77065683 | Rare:50 | ||||
| chr12:78864426-78864822 | Common:2; Rare:88 | ||||
| chr12:79934451-79934651 | Rare:51 | ||||
| chr12:79934901-79935399 | Common:1; Rare:189 | ||||
| chr12:82358222-82358555 | Common:2; Rare:163 | ||||
| chr12:82358712-82358903 | Common:3; Rare:100 |