| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188977-49189171 | Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49189176-49189281 | Rare:23 | ||||
| chr12:49264768-49265184 | Common:4; Rare:159 | ||||
| chr12:49322960-49323335 | Common:3; Rare:91 | ||||
| chr12:49367263-49367586 | Common:1; Rare:84 | ||||
| chr12:49567839-49568234 | Common:2; Rare:108 | ||||
| chr12:49623238-49623591 | Common:2; Rare:100 | ||||
| chr12:49707460-49707763 | Rare:83 | ||||
| chr12:49741230-49741626 | Rare:112 | ||||
| chr12:49828374-49828600 | Common:1; Rare:86 | ||||
| chr12:49843059-49843219 | Common:2; Rare:62; Clinvar (benign):1 | ||||
| chr12:50025359-50025779 | Common:2; Rare:115 | ||||
| chr12:50085043-50085392 | Common:1; Rare:93 | ||||
| chr12:50085457-50085537 | Rare:14 | ||||
| chr12:50086105-50086231 | Common:1; Rare:28 |