| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6770156-6770517 | Rare:105 | ||||
| chr12:6927548-6927794 | Rare:63 | ||||
| chr12:6933563-6933859 | Rare:61 | ||||
| chr12:6933938-6934212 | Rare:74 | ||||
| chr12:8242933-8243180 | Common:5; Rare:73 | ||||
| chr12:9065063-9065186 | Rare:13 | ||||
| chr12:9069799-9070006 | Rare:49 | ||||
| chr12:9070486-9070808 | Common:1; Rare:61 | ||||
| chr12:9072652-9073096 | Rare:104 | ||||
| chr12:9093468-9093710 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr12:9104238-9104654 | Common:4; Rare:86 | ||||
| chr12:9107522-9107780 | Common:4; Rare:53 | ||||
| chr12:9109319-9109526 | Rare:47 | ||||
| chr12:9112375-9112670 | Rare:72 | ||||
| chr12:9240337-9240394 | Common:1; Rare:11 |