| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6383988-6384268 | Common:1; Rare:62 | ||||
| chr12:6493208-6493381 | Common:6; Rare:48 | ||||
| chr12:6493746-6494132 | Common:2; Rare:115 | ||||
| chr12:6568234-6568382 | Rare:55 | ||||
| chr12:6688884-6689089 | Rare:68 | ||||
| chr12:6689467-6689748 | Common:1; Rare:70 | ||||
| chr12:6723963-6724172 | Rare:55 | ||||
| chr12:6851887-6852193 | Rare:80 | ||||
| chr12:6867387-6867561 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873291-6873541 | Common:1; Rare:73 | ||||
| chr12:6970602-6970952 | Common:3; Rare:107 | ||||
| chr12:7130309-7130423 | Common:4; Rare:28 | ||||
| chr12:8949583-8949691 | Rare:29 | ||||
| chr12:9079764-9080006 | Rare:50 | ||||
| chr12:9760893-9761003 | Rare:14 |