| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:79690854-79691221 | Common:1; Rare:122 | ||||
| chr12:79691376-79691548 | Rare:41 | ||||
| chr12:79820776-79821084 | Rare:69 | ||||
| chr12:79934912-79935420 | Common:1; Rare:190 | ||||
| chr12:82358224-82358589 | Common:2; Rare:188 | ||||
| chr12:82358733-82358906 | Common:3; Rare:87 | ||||
| chr12:82686630-82686929 | Rare:85 | ||||
| chr12:84912706-84912965 | Common:1; Rare:62 | ||||
| chr12:85036249-85036381 | Rare:33 | ||||
| chr12:85836204-85836258 | Common:1; Rare:15 | ||||
| chr12:85836272-85836432 | Rare:22 | ||||
| chr12:88035368-88035667 | Common:1; Rare:82 | ||||
| chr12:88141777-88142166 | Common:2; Rare:83; Clinvar:7; Clinvar (benign):1 | ||||
| chr12:88142194-88142526 | Common:2; Rare:87 | ||||
| chr12:88580400-88580586 | Common:2; Rare:64 |