| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188488-49188590 | Common:1; Rare:14 | ||||
| chr12:49322980-49323302 | Common:3; Rare:73 | ||||
| chr12:49367212-49367530 | Common:1; Rare:88 | ||||
| chr12:49568104-49568192 | Common:2; Rare:29 | ||||
| chr12:49741258-49741607 | Rare:99 | ||||
| chr12:49758245-49758454 | Common:4; Rare:63 | ||||
| chr12:49828398-49828626 | Rare:80 | ||||
| chr12:50167296-50167699 | Common:3; Rare:107 | ||||
| chr12:50283473-50283665 | Common:2; Rare:61 | ||||
| chr12:51026319-51026545 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51238648-51238890 | Common:8; Rare:104 | ||||
| chr12:51270278-51270347 | Common:2; Rare:18 | ||||
| chr12:52051140-52051448 | Common:1; Rare:101 | ||||
| chr12:52949784-52950019 | Rare:53 | ||||
| chr12:53006102-53006486 | Common:4; Rare:144 |