| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49741268-49741607 | Rare:95 | ||||
| chr12:49750499-49750675 | Rare:30 | ||||
| chr12:49828387-49828595 | Common:1; Rare:77 | ||||
| chr12:49843083-49843200 | Common:1; Rare:46 | ||||
| chr12:50025366-50025758 | Common:2; Rare:106 | ||||
| chr12:50085026-50085399 | Common:1; Rare:100 | ||||
| chr12:50111727-50112105 | Common:1; Rare:77 | ||||
| chr12:50167298-50167597 | Common:3; Rare:91 | ||||
| chr12:50283490-50283672 | Common:3; Rare:57 | ||||
| chr12:50400719-50400988 | Common:1; Rare:85 | ||||
| chr12:50401298-50401432 | Common:1; Rare:31 | ||||
| chr12:50504851-50505118 | Common:3; Rare:111 | ||||
| chr12:50763914-50764297 | Common:1; Rare:103 | ||||
| chr12:50764321-50764522 | Common:4; Rare:68 | ||||
| chr12:51026313-51026553 | Common:3; Rare:102; Clinvar:2; Clinvar (benign):2 |