| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6362013-6362083 | Rare:28; Clinvar (pathogenic):1 | ||||
| chr12:6375161-6375723 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376120-6376278 | Common:2; Rare:36 | ||||
| chr12:6451117-6451273 | Common:1; Rare:30 | ||||
| chr12:6451809-6452120 | Common:4; Rare:59 | ||||
| chr12:6470630-6470875 | Common:1; Rare:77 | ||||
| chr12:6493202-6493394 | Common:6; Rare:52 | ||||
| chr12:6493770-6494144 | Common:2; Rare:111 | ||||
| chr12:6533506-6533599 | Rare:19 | ||||
| chr12:6533896-6534171 | Common:3; Rare:49 | ||||
| chr12:6534270-6534861 | Common:8; Rare:241 | ||||
| chr12:6535157-6535410 | Common:3; Rare:80 | ||||
| chr12:6535419-6535700 | Common:5; Rare:77 | ||||
| chr12:6567798-6568216 | Common:1; Rare:133 | ||||
| chr12:6568224-6568371 | Rare:53 |