| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501556-21501866 | Common:2; Rare:79 | ||||
| chr12:22544509-22544677 | Common:1; Rare:35 | ||||
| chr12:24949020-24949139 | Rare:30 | ||||
| chr12:25195128-25195308 | Common:2; Rare:53 | ||||
| chr12:26937936-26938526 | Common:11; Rare:192 | ||||
| chr12:27523990-27524270 | Rare:66 | ||||
| chr12:28190367-28190483 | Common:1; Rare:34 | ||||
| chr12:31073722-31073907 | Common:8; Rare:63 | ||||
| chr12:31729012-31729290 | Common:1; Rare:83 | ||||
| chr12:31959262-31959482 | Common:2; Rare:70 | ||||
| chr12:32679101-32679335 | Common:1; Rare:90; Clinvar (benign):2 | ||||
| chr12:32755471-32755510 | Rare:12 | ||||
| chr12:32896709-32896980 | Common:2; Rare:90; Clinvar:6; Clinvar (benign):7 | ||||
| chr12:42325958-42326206 | Common:1; Rare:78 | ||||
| chr12:43758745-43758996 | Common:2; Rare:69; Clinvar:2 |