| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:81077987-81078140 | Rare:35 | ||||
| chr12:82357940-82358168 | Common:1; Rare:73 | ||||
| chr12:82358222-82358582 | Common:2; Rare:183 | ||||
| chr12:82358724-82358915 | Common:3; Rare:96 | ||||
| chr12:82686710-82686919 | Rare:67 | ||||
| chr12:84912554-84912903 | Common:1; Rare:76 | ||||
| chr12:85036243-85036371 | Rare:31 | ||||
| chr12:88035432-88035640 | Common:1; Rare:67 | ||||
| chr12:88141779-88141933 | Common:2; Rare:27; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:88141973-88142471 | Common:1; Rare:139; Clinvar:5 | ||||
| chr12:88580432-88580581 | Common:2; Rare:52 | ||||
| chr12:89352235-89352747 | Common:1; Rare:145 | ||||
| chr12:89353651-89353750 | Common:3; Rare:23 | ||||
| chr12:89524716-89524887 | Common:1; Rare:32 | ||||
| chr12:89525406-89525621 | Common:1; Rare:51 |