| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45990429-45990995 | Common:6; Rare:329 | ||||
| chr12:45991988-45992204 | Common:4; Rare:65 | ||||
| chr12:46268445-46269260 | Common:5; Rare:327 | ||||
| chr12:46372107-46372507 | Common:1; Rare:167 | ||||
| chr12:46372509-46373065 | Common:2; Rare:329 | ||||
| chr12:46825943-46826081 | Common:1; Rare:35 | ||||
| chr12:47705947-47706132 | Rare:148 | ||||
| chr12:47819843-47820055 | Common:2; Rare:87 | ||||
| chr12:47904981-47905127 | Common:2; Rare:80; Clinvar:2 | ||||
| chr12:48004444-48004986 | Common:4; Rare:201; Clinvar (benign):2 | ||||
| chr12:48105610-48105940 | Common:5; Rare:100 | ||||
| chr12:48105949-48106320 | Common:4; Rare:193 | ||||
| chr12:48350846-48351082 | Common:5; Rare:85 | ||||
| chr12:48682196-48682471 | Common:9; Rare:153 | ||||
| chr12:48716662-48716945 | Common:8; Rare:173 |