| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57771773-57771940 | Rare:38 | ||||
| chr12:57772017-57772387 | Common:1; Rare:111 | ||||
| chr12:57772458-57772665 | Common:2; Rare:41 | ||||
| chr12:57782445-57782880 | Common:3; Rare:122; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57845104-57845398 | Common:2; Rare:73 | ||||
| chr12:57845560-57845727 | Common:2; Rare:46 | ||||
| chr12:57845786-57845878 | Common:1; Rare:21 | ||||
| chr12:57846926-57847222 | Common:2; Rare:110 | ||||
| chr12:57941094-57941632 | Common:5; Rare:138 | ||||
| chr12:57941635-57941813 | Rare:53 | ||||
| chr12:58919490-58919641 | Common:1; Rare:36 | ||||
| chr12:59595772-59596088 | Common:7; Rare:67 | ||||
| chr12:59596551-59596790 | Common:2; Rare:47 | ||||
| chr12:59596904-59597121 | Common:2; Rare:51 | ||||
| chr12:59597471-59597512 | Common:2; Rare:6 |