| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56604215-56604559 | Rare:72 | ||||
| chr12:56617507-56617578 | Rare:17 | ||||
| chr12:56634966-56635112 | Common:1; Rare:25 | ||||
| chr12:56991418-56991720 | Common:1; Rare:57 | ||||
| chr12:57162658-57162976 | Rare:71 | ||||
| chr12:57184130-57184437 | Rare:74 | ||||
| chr12:57195769-57195989 | Common:1; Rare:55 | ||||
| chr12:57210473-57210860 | Common:1; Rare:87 | ||||
| chr12:57211926-57212165 | Common:1; Rare:62 | ||||
| chr12:57462804-57463106 | Common:2; Rare:57 | ||||
| chr12:62389446-62389646 | Rare:50 | ||||
| chr12:62603541-62603622 | Common:1; Rare:27 | ||||
| chr12:63821851-63821959 | Rare:34 | ||||
| chr12:64720157-64720413 | Common:2; Rare:42; Clinvar:1 | ||||
| chr12:64737012-64737213 | Rare:46; Clinvar:1; Clinvar (pathogenic):1 |