| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372734-46372965 | Rare:98 | ||||
| chr12:47705967-47706170 | Rare:75 | ||||
| chr12:47758910-47759320 | Common:5; Rare:76 | ||||
| chr12:47773084-47773260 | Rare:65 | ||||
| chr12:47812956-47813356 | Rare:143 | ||||
| chr12:47818945-47819508 | Common:5; Rare:174 | ||||
| chr12:47819871-47820089 | Common:1; Rare:52 | ||||
| chr12:47820747-47821060 | Common:2; Rare:53 | ||||
| chr12:47963399-47963652 | Common:2; Rare:61 | ||||
| chr12:48004472-48004684 | Common:2; Rare:43; Clinvar (benign):1 | ||||
| chr12:48004809-48004918 | Rare:26 | ||||
| chr12:48105788-48106230 | Common:3; Rare:132 | ||||
| chr12:48106276-48106469 | Rare:51 | ||||
| chr12:48119165-48119402 | Common:2; Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119619-48120180 | Common:3; Rare:156 |