| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54430959-54431180 | Common:2; Rare:54 | ||||
| chr19:54435251-54435553 | Common:2; Rare:78 | ||||
| chr19:54448586-54448634 | Rare:7 | ||||
| chr19:54449012-54449298 | Common:4; Rare:86 | ||||
| chr19:54449370-54449717 | Common:8; Rare:108 | ||||
| chr19:54451184-54451380 | Common:3; Rare:51 | ||||
| chr19:54451420-54451536 | Common:1; Rare:29 | ||||
| chr19:54966241-54966404 | Common:2; Rare:47 | ||||
| chr19:55092235-55092526 | Rare:113 | ||||
| chr19:55094603-55094702 | Rare:38 | ||||
| chr19:55146451-55146650 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr19:55146683-55146724 | Common:1; Rare:9; Clinvar (benign):2 | ||||
| chr19:55156426-55156531 | Common:1; Rare:35 | ||||
| chr19:55160663-55160872 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:55160913-55161032 | Common:2; Rare:29 |