| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53999637-53999844 | Rare:56 | ||||
| chr12:53999949-54000161 | Common:4; Rare:58 | ||||
| chr12:54017169-54017205 | Rare:5 | ||||
| chr12:54280063-54280320 | Rare:86 | ||||
| chr12:54281774-54282179 | Common:1; Rare:103; Clinvar (benign):1 | ||||
| chr12:54391240-54391471 | Rare:52 | ||||
| chr12:55716010-55716195 | Common:1; Rare:87 | ||||
| chr12:55716250-55716524 | Common:1; Rare:67 | ||||
| chr12:55728275-55728495 | Rare:74 | ||||
| chr12:55728961-55729138 | Rare:33 | ||||
| chr12:55729659-55729790 | Rare:29 | ||||
| chr12:55829497-55829795 | Rare:92 | ||||
| chr12:55830782-55830957 | Common:1; Rare:50 | ||||
| chr12:55966031-55966232 | Common:1; Rare:38 | ||||
| chr12:55966556-55966890 | Rare:83 |