| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57823601-57823914 | Rare:83 | ||||
| chr12:57836906-57837114 | Common:1; Rare:30 | ||||
| chr12:57936014-57936202 | Common:3; Rare:52 | ||||
| chr12:62603493-62603647 | Common:1; Rare:50 | ||||
| chr12:64682634-64682818 | Common:4; Rare:30 | ||||
| chr12:69624046-69624420 | Rare:87 | ||||
| chr12:77324783-77325024 | Common:2; Rare:82 | ||||
| chr12:93174142-93174356 | Common:3; Rare:32 | ||||
| chr12:98503835-98504012 | Common:2; Rare:50 | ||||
| chr12:101680230-101680501 | Rare:68; Clinvar (benign):1 | ||||
| chr12:103946334-103946696 | Common:4; Rare:93 | ||||
| chr12:104858735-104858863 | Rare:26 | ||||
| chr12:108802189-108802430 | Rare:36 | ||||
| chr12:108838384-108838581 | Common:1; Rare:41 | ||||
| chr12:109111039-109111224 | Common:1; Rare:53 |