| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48851975-48852471 | Common:8; Rare:344 | ||||
| chr12:48865814-48866082 | Common:1; Rare:106 | ||||
| chr12:48924749-48924883 | Common:2; Rare:23 | ||||
| chr12:48956320-48956756 | Common:9; Rare:187 | ||||
| chr12:48957313-48957632 | Common:8; Rare:224 | ||||
| chr12:49018435-49019188 | Common:7; Rare:391; Clinvar (benign):3 | ||||
| chr12:49058554-49059441 | Common:1; Rare:212 | ||||
| chr12:49059922-49060051 | Rare:25 | ||||
| chr12:49060150-49060420 | Rare:187 | ||||
| chr12:49069450-49069810 | Common:14; Rare:164 | ||||
| chr12:49069830-49070220 | Common:6; Rare:208 | ||||
| chr12:49110588-49111140 | Rare:293 | ||||
| chr12:49130164-49130564 | Common:1; Rare:193 | ||||
| chr12:49130629-49131037 | Common:14; Rare:349 | ||||
| chr12:49131303-49131745 | Common:6; Rare:424 |