| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48815430-48815596 | Common:1; Rare:40 | ||||
| chr12:49018735-49018851 | Rare:55 | ||||
| chr12:49131355-49131592 | Rare:88 | ||||
| chr12:49189049-49189274 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:49568104-49568171 | Common:1; Rare:22 | ||||
| chr12:49828407-49828543 | Rare:44 | ||||
| chr12:49843095-49843168 | Rare:26 | ||||
| chr12:49903855-49904094 | Common:2; Rare:60 | ||||
| chr12:50283496-50283632 | Rare:39 | ||||
| chr12:51048103-51048359 | Common:2; Rare:87 | ||||
| chr12:51238668-51238913 | Common:4; Rare:106 | ||||
| chr12:51239121-51239306 | Common:2; Rare:55 | ||||
| chr12:52051123-52051449 | Common:1; Rare:108 | ||||
| chr12:53049748-53050085 | Rare:80 | ||||
| chr12:53079344-53079559 | Common:2; Rare:74 |