| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47749929-47750149 | Common:1; Rare:65 | ||||
| chr12:47789573-47789707 | Rare:21 | ||||
| chr12:48134819-48135006 | Rare:51; Clinvar (benign):1 | ||||
| chr12:48143797-48144103 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:48758820-48758997 | Rare:27 | ||||
| chr12:48775327-48775536 | Common:1; Rare:58 | ||||
| chr12:48785998-48786141 | Common:1; Rare:20 | ||||
| chr12:49009274-49009326 | Rare:6 | ||||
| chr12:49028887-49029086 | Common:3; Rare:57; Clinvar (benign):2 | ||||
| chr12:49042817-49043061 | Common:1; Rare:66; Clinvar:2 | ||||
| chr12:49060734-49060913 | Common:1; Rare:69 | ||||
| chr12:49633708-49634030 | Common:1; Rare:74 | ||||
| chr12:49635684-49635918 | Common:1; Rare:55 | ||||
| chr12:49649832-49649989 | Common:2; Rare:36 | ||||
| chr12:50192533-50192707 | Rare:29 |