| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46383903-46384047 | Rare:43 | ||||
| chr12:46409257-46409299 | Rare:9 | ||||
| chr12:47789573-47789845 | Rare:52 | ||||
| chr12:47818332-47818605 | Common:1; Rare:43 | ||||
| chr12:47821377-47821483 | Common:3; Rare:16 | ||||
| chr12:48198126-48198385 | Common:4; Rare:66 | ||||
| chr12:49060769-49061027 | Common:1; Rare:80 | ||||
| chr12:49755433-49755714 | Common:1; Rare:62 | ||||
| chr12:50106017-50106309 | Common:3; Rare:54 | ||||
| chr12:50106810-50107120 | Rare:88 | ||||
| chr12:50109212-50109541 | Common:3; Rare:60 | ||||
| chr12:50221326-50221460 | Rare:23 | ||||
| chr12:50929706-50930016 | Common:1; Rare:73 | ||||
| chr12:51913336-51913575 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:51952330-51952487 | Rare:46 |