| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372592-46372852 | Rare:113 | ||||
| chr12:47079481-47079650 | Common:1; Rare:36 | ||||
| chr12:47705955-47706088 | Rare:60 | ||||
| chr12:47904984-47905131 | Common:1; Rare:42; Clinvar:1 | ||||
| chr12:48105825-48106139 | Common:1; Rare:92 | ||||
| chr12:48716666-48716884 | Common:4; Rare:72 | ||||
| chr12:48789037-48789312 | Rare:56 | ||||
| chr12:48815457-48815624 | Common:1; Rare:37 | ||||
| chr12:49003508-49003770 | Common:1; Rare:70 | ||||
| chr12:49018733-49018911 | Rare:70 | ||||
| chr12:49131304-49131606 | Common:2; Rare:123 | ||||
| chr12:49188975-49189356 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264729-49265123 | Common:5; Rare:138 | ||||
| chr12:49269648-49269871 | Common:2; Rare:79 | ||||
| chr12:49567850-49568218 | Common:2; Rare:100 |