| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49131348-49131614 | Common:2; Rare:101 | ||||
| chr12:49188975-49189296 | Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265092 | Common:4; Rare:111 | ||||
| chr12:49322980-49323311 | Common:3; Rare:78 | ||||
| chr12:49568104-49568188 | Common:2; Rare:26 | ||||
| chr12:49623284-49623579 | Common:1; Rare:82 | ||||
| chr12:49741275-49741611 | Rare:94 | ||||
| chr12:49750531-49750664 | Rare:21 | ||||
| chr12:49828353-49828594 | Common:1; Rare:91 | ||||
| chr12:50085064-50085399 | Common:1; Rare:92 | ||||
| chr12:50283433-50283664 | Common:2; Rare:68 | ||||
| chr12:50400716-50401008 | Common:1; Rare:95 | ||||
| chr12:50763805-50764124 | Common:2; Rare:94 | ||||
| chr12:51026328-51026496 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51238648-51238915 | Common:8; Rare:115 |