| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57265680-57265855 | Common:2; Rare:25 | ||||
| chr12:57272970-57273132 | Rare:25 | ||||
| chr12:57735531-57735718 | Common:1; Rare:31 | ||||
| chr12:57750916-57751316 | Common:1; Rare:114; Clinvar:22; Clinvar (benign):21 | ||||
| chr12:57823620-57823914 | Rare:81 | ||||
| chr12:57868885-57869047 | Rare:31 | ||||
| chr12:57888744-57888965 | Rare:36 | ||||
| chr12:57893903-57893976 | Rare:9 | ||||
| chr12:57935863-57936262 | Common:4; Rare:93 | ||||
| chr12:59084914-59085099 | Common:1; Rare:39 | ||||
| chr12:60872900-60873024 | Rare:20 | ||||
| chr12:66190873-66190944 | Rare:10 | ||||
| chr12:66242444-66242606 | Common:1; Rare:27 | ||||
| chr12:68794154-68794277 | Common:1; Rare:9 | ||||
| chr12:70468027-70468126 | Common:1; Rare:23 |