| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54259527-54259724 | Rare:38 | ||||
| chr12:54283718-54284068 | Common:1; Rare:100; Clinvar:2; Clinvar (pathogenic):6 | ||||
| chr12:54300874-54301144 | Rare:52 | ||||
| chr12:54385715-54385984 | Rare:52 | ||||
| chr12:54403913-54404154 | Rare:55 | ||||
| chr12:54413215-54413315 | Rare:17 | ||||
| chr12:54419065-54419112 | Rare:19 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:54561197-54561538 | Common:1; Rare:53 | ||||
| chr12:54984682-54984833 | Rare:27 | ||||
| chr12:55707505-55707538 | Rare:8; Clinvar:2 | ||||
| chr12:55712265-55712382 | Common:2; Rare:25 | ||||
| chr12:55715613-55715663 | Rare:9 | ||||
| chr12:55715997-55716195 | Common:2; Rare:93 | ||||
| chr12:55716734-55716977 | Rare:54 |