| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49741258-49741668 | Rare:192 | ||||
| chr12:49741987-49742205 | Rare:83 | ||||
| chr12:49827668-49828068 | Common:4; Rare:138 | ||||
| chr12:49828352-49828720 | Common:3; Rare:257 | ||||
| chr12:49842688-49843278 | Common:8; Rare:390; Clinvar (benign):3 | ||||
| chr12:49966930-49967369 | Common:8; Rare:207 | ||||
| chr12:50025336-50025834 | Common:6; Rare:329 | ||||
| chr12:50057251-50057738 | Common:3; Rare:196 | ||||
| chr12:50070490-50070820 | Common:4; Rare:110 | ||||
| chr12:50085012-50085414 | Common:3; Rare:298 | ||||
| chr12:50085425-50086062 | Common:5; Rare:243 | ||||
| chr12:50111728-50112306 | Common:6; Rare:255 | ||||
| chr12:50112550-50113060 | Common:12; Rare:179 | ||||
| chr12:50137594-50138035 | Rare:172 | ||||
| chr12:50144842-50145389 | Common:8; Rare:171 |