| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74291747-74292272 | Common:5; Rare:161; Clinvar:1 | ||||
| chr18:74496021-74496434 | Common:4; Rare:132 | ||||
| chr18:74499750-74500032 | Common:2; Rare:72 | ||||
| chr18:74597584-74597914 | Common:2; Rare:88 | ||||
| chr18:75210723-75210887 | Rare:30; Clinvar:1 | ||||
| chr18:76822236-76822596 | Common:11; Rare:101 | ||||
| chr18:79988339-79988661 | Common:4; Rare:112; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572311-572661 | Common:1; Rare:180 | ||||
| chr19:619268-619588 | Common:5; Rare:155 | ||||
| chr19:633467-633626 | Common:8; Rare:92 | ||||
| chr19:663099-663426 | Common:3; Rare:125 | ||||
| chr19:680459-680754 | Common:2; Rare:101 | ||||
| chr19:893155-893484 | Common:3; Rare:140 | ||||
| chr19:984277-984414 | Rare:51 | ||||
| chr19:1021207-1021581 | Common:15; Rare:184 |