| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188981-49189227 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265181 | Common:4; Rare:156 | ||||
| chr12:49322986-49323264 | Common:2; Rare:61 | ||||
| chr12:49367229-49367556 | Common:1; Rare:86 | ||||
| chr12:49568078-49568253 | Common:2; Rare:57 | ||||
| chr12:49623284-49623586 | Common:1; Rare:82 | ||||
| chr12:49741391-49741611 | Rare:66 | ||||
| chr12:49750503-49750626 | Rare:20 | ||||
| chr12:49828362-49828554 | Common:1; Rare:71 | ||||
| chr12:49843092-49843176 | Rare:29 | ||||
| chr12:50085296-50085381 | Common:1; Rare:17 | ||||
| chr12:50103881-50104053 | Rare:44 | ||||
| chr12:50112129-50112291 | Common:1; Rare:38 | ||||
| chr12:50167293-50167624 | Common:3; Rare:97 | ||||
| chr12:50283433-50283672 | Common:3; Rare:72 |