| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53230630-53230871 | Common:1; Rare:44 | ||||
| chr12:54081813-54081987 | Common:1; Rare:33 | ||||
| chr12:54429030-54429424 | Common:2; Rare:74 | ||||
| chr12:56190254-56190330 | Common:1; Rare:40 | ||||
| chr12:56634966-56635116 | Common:1; Rare:27 | ||||
| chr12:57162685-57162899 | Rare:46 | ||||
| chr12:57194501-57194683 | Common:1; Rare:49 | ||||
| chr12:57546046-57546245 | Rare:43 | ||||
| chr12:57751011-57751263 | Common:1; Rare:76; Clinvar:14; Clinvar (benign):10 | ||||
| chr12:62603432-62603614 | Common:1; Rare:68 | ||||
| chr12:71710327-71710432 | Rare:26 | ||||
| chr12:76030531-76030788 | Rare:113 | ||||
| chr12:76030799-76031074 | Common:1; Rare:89 | ||||
| chr12:76863235-76863573 | Rare:80 | ||||
| chr12:103946460-103946860 | Common:1; Rare:106 |