| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76031593-76031875 | Common:1; Rare:88 | ||||
| chr12:76083928-76084041 | Rare:36 | ||||
| chr12:76084565-76084857 | Common:1; Rare:95 | ||||
| chr12:76348342-76348502 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559690-76560074 | Common:2; Rare:124 | ||||
| chr12:76764046-76764269 | Common:2; Rare:92 | ||||
| chr12:76878987-76879248 | Rare:88 | ||||
| chr12:79782498-79782662 | Rare:34 | ||||
| chr12:79934694-79935319 | Common:1; Rare:215 | ||||
| chr12:79935328-79935396 | Rare:17 | ||||
| chr12:80937651-80937871 | Common:1; Rare:68 | ||||
| chr12:80937902-80938196 | Common:1; Rare:52 | ||||
| chr12:82358372-82358568 | Rare:87 | ||||
| chr12:82358693-82358906 | Common:3; Rare:109 | ||||
| chr12:85836203-85836258 | Common:1; Rare:15 |