| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48105972-48106179 | Common:2; Rare:67 | ||||
| chr12:48106277-48106388 | Rare:37 | ||||
| chr12:48183551-48183635 | Common:1; Rare:22 | ||||
| chr12:48350833-48350950 | Rare:46 | ||||
| chr12:48682187-48682431 | Common:5; Rare:80 | ||||
| chr12:48716665-48716955 | Common:4; Rare:92 | ||||
| chr12:48818348-48818525 | Rare:66 | ||||
| chr12:48852085-48852180 | Rare:37 | ||||
| chr12:48865840-48866085 | Common:1; Rare:64 | ||||
| chr12:48957297-48957645 | Common:4; Rare:98 | ||||
| chr12:49018736-49019035 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr12:49069922-49070142 | Common:2; Rare:56 | ||||
| chr12:49110619-49111062 | Rare:98 | ||||
| chr12:49131296-49131614 | Common:2; Rare:125 | ||||
| chr12:49188462-49188639 | Common:2; Rare:22 |