| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56235856-56236126 | Common:3; Rare:49 | ||||
| chr12:56634966-56635122 | Common:1; Rare:27 | ||||
| chr12:57046571-57046920 | Rare:101; Clinvar (benign):2 | ||||
| chr12:57165790-57165819 | Rare:7 | ||||
| chr12:57195770-57196165 | Common:3; Rare:107 | ||||
| chr12:57546042-57546211 | Rare:38 | ||||
| chr12:57823600-57823914 | Rare:84 | ||||
| chr12:57882631-57882811 | Rare:20 | ||||
| chr12:57888550-57888687 | Rare:29 | ||||
| chr12:65170135-65170202 | Rare:19 | ||||
| chr12:67710721-67710886 | Rare:24 | ||||
| chr12:67715632-67715694 | Rare:3 | ||||
| chr12:71153019-71153118 | Rare:26 | ||||
| chr12:89359122-89359180 | Common:2; Rare:12 | ||||
| chr12:89960130-89960295 | Rare:18 |