| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64459304-64459704 | Common:1; Rare:84 | ||||
| chr12:64608772-64609172 | Common:3; Rare:122 | ||||
| chr12:64611023-64611244 | Common:1; Rare:61 | ||||
| chr12:64612049-64612300 | Rare:110 | ||||
| chr12:64619220-64619468 | Rare:44 | ||||
| chr12:64621110-64621514 | Common:8; Rare:153 | ||||
| chr12:64625373-64625514 | Common:2; Rare:50 | ||||
| chr12:64625750-64626205 | Common:3; Rare:156 | ||||
| chr12:64665438-64665758 | Common:1; Rare:61 | ||||
| chr12:64669313-64669713 | Common:9; Rare:110 | ||||
| chr12:64669700-64670230 | Common:6; Rare:137 | ||||
| chr12:64714676-64715076 | Common:1; Rare:108; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:64730254-64730654 | Common:8; Rare:80 | ||||
| chr12:64756420-64756670 | Common:2; Rare:47 | ||||
| chr12:64800630-64801070 | Common:1; Rare:114 |