| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49828379-49828536 | Common:1; Rare:58 | ||||
| chr12:50283475-50283672 | Common:3; Rare:63 | ||||
| chr12:50763920-50764128 | Common:1; Rare:59 | ||||
| chr12:51048103-51048351 | Common:2; Rare:83 | ||||
| chr12:51238666-51238910 | Common:5; Rare:107 | ||||
| chr12:52043476-52043725 | Common:3; Rare:55 | ||||
| chr12:52051152-52051493 | Common:1; Rare:111 | ||||
| chr12:52191919-52192047 | Common:1; Rare:35 | ||||
| chr12:52520388-52520609 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:53049948-53050100 | Rare:45 | ||||
| chr12:53079372-53079568 | Common:2; Rare:59 | ||||
| chr12:53097390-53097687 | Rare:61 | ||||
| chr12:53180610-53180768 | Common:1; Rare:60 | ||||
| chr12:53180896-53181150 | Common:4; Rare:71 | ||||
| chr12:53181306-53181443 | Rare:32 |