| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49130296-49130528 | Common:1; Rare:92 | ||||
| chr12:49130676-49131032 | Common:5; Rare:125 | ||||
| chr12:49131243-49131745 | Common:2; Rare:189 | ||||
| chr12:49187281-49187365 | Rare:17 | ||||
| chr12:49188875-49189399 | Common:1; Rare:131; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264735-49265216 | Common:6; Rare:173 | ||||
| chr12:49265504-49265584 | Rare:18 | ||||
| chr12:49322889-49323347 | Common:5; Rare:114 | ||||
| chr12:49337146-49337363 | Common:2; Rare:48 | ||||
| chr12:49347161-49347213 | Common:1; Rare:9 | ||||
| chr12:49366093-49366405 | Common:3; Rare:61 | ||||
| chr12:49366431-49366465 | Common:1; Rare:12 | ||||
| chr12:49366575-49367554 | Common:4; Rare:256 | ||||
| chr12:49367714-49367798 | Common:2; Rare:17 | ||||
| chr12:49367996-49368073 | Rare:14 |