| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48118496-48118896 | Common:5; Rare:92 | ||||
| chr12:48119074-48119474 | Common:6; Rare:154; Clinvar:11; Clinvar (benign):6 | ||||
| chr12:48156755-48157215 | Common:2; Rare:133 | ||||
| chr12:48157117-48158365 | Common:27; Rare:814 | ||||
| chr12:48182972-48183372 | Common:3; Rare:75 | ||||
| chr12:48350222-48350670 | Common:4; Rare:155 | ||||
| chr12:48350700-48351170 | Common:30; Rare:688 | ||||
| chr12:48351076-48351768 | Common:9; Rare:390 | ||||
| chr12:48681529-48682027 | Rare:294 | ||||
| chr12:48682120-48682631 | Common:32; Rare:554 | ||||
| chr12:48716476-48717220 | Common:35; Rare:984 | ||||
| chr12:48789000-48789500 | Common:2; Rare:172 | ||||
| chr12:48814070-48814204 | Rare:20 | ||||
| chr12:48814193-48814522 | Common:6; Rare:99 | ||||
| chr12:48814536-48815000 | Rare:356 |