| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064027-104064202 | Rare:37 | ||||
| chr12:104064327-104064691 | Common:1; Rare:91 | ||||
| chr12:104138147-104138384 | Common:1; Rare:61 | ||||
| chr12:104286900-104287341 | Common:3; Rare:98 | ||||
| chr12:104288835-104289036 | Rare:85 | ||||
| chr12:104309429-104309490 | Common:1; Rare:7 | ||||
| chr12:104334238-104334667 | Common:1; Rare:103 | ||||
| chr12:104958258-104958380 | Common:3; Rare:35 | ||||
| chr12:105107609-105107852 | Common:1; Rare:104; Clinvar:1 | ||||
| chr12:105152375-105152505 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr12:105195222-105195282 | Rare:21 | ||||
| chr12:105235964-105236265 | Common:3; Rare:116 | ||||
| chr12:105330664-105330935 | Common:3; Rare:87 | ||||
| chr12:105331340-105331443 | Rare:16 | ||||
| chr12:106084070-106084276 | Common:2; Rare:32 |