| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:1753175-1753347 | Rare:37 | ||||
| chr12:1766138-1766402 | Common:1; Rare:33 | ||||
| chr12:1767666-1767787 | Common:1; Rare:22 | ||||
| chr12:1767740-1768305 | Common:4; Rare:123 | ||||
| chr12:1776566-1777105 | Common:1; Rare:204 | ||||
| chr12:1794701-1795021 | Common:3; Rare:66 | ||||
| chr12:1836690-1837220 | Common:4; Rare:130 | ||||
| chr12:1837180-1837450 | Common:1; Rare:60 | ||||
| chr12:1840030-1840660 | Common:14; Rare:183 | ||||
| chr12:1841512-1841874 | Common:2; Rare:55 | ||||
| chr12:1907611-1907915 | Common:4; Rare:83; Clinvar:2 | ||||
| chr12:2034373-2035293 | Common:16; Rare:347 | ||||
| chr12:2161530-2162130 | Common:4; Rare:121 | ||||
| chr12:2286119-2286519 | Common:1; Rare:82 | ||||
| chr12:2797237-2797415 | Common:1; Rare:48 |