| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018524-49018960 | Common:4; Rare:156 | ||||
| chr12:49019293-49019361 | Rare:9 | ||||
| chr12:49059404-49059641 | Rare:46 | ||||
| chr12:49059873-49060034 | Rare:33 | ||||
| chr12:49060179-49060472 | Rare:75 | ||||
| chr12:49069567-49069776 | Common:6; Rare:59 | ||||
| chr12:49069881-49070196 | Common:2; Rare:73 | ||||
| chr12:49110562-49111084 | Rare:130 | ||||
| chr12:49130239-49130524 | Common:1; Rare:108 | ||||
| chr12:49130708-49131034 | Common:5; Rare:119 | ||||
| chr12:49131256-49131730 | Common:2; Rare:178 | ||||
| chr12:49188994-49189295 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264509-49265216 | Common:8; Rare:217 | ||||
| chr12:49265504-49265726 | Common:1; Rare:43 | ||||
| chr12:49297303-49297397 | Rare:29 |