| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37078177-37078483 | Common:4; Rare:71 | ||||
| chr19:37467190-37467519 | Common:2; Rare:95 | ||||
| chr19:37551270-37551389 | Rare:42 | ||||
| chr19:37594760-37594905 | Rare:38 | ||||
| chr19:38831765-38832061 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr19:38899528-38900033 | Rare:154 | ||||
| chr19:38930723-38930988 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39391025-39391418 | Common:1; Rare:158 | ||||
| chr19:39480597-39480931 | Common:3; Rare:162; Clinvar (pathogenic):1 | ||||
| chr19:39846335-39846468 | Common:1; Rare:59 | ||||
| chr19:39970938-39971200 | Common:4; Rare:73 | ||||
| chr19:40056157-40056262 | Rare:15 | ||||
| chr19:40090886-40090976 | Common:1; Rare:25 | ||||
| chr19:40348377-40348739 | Common:4; Rare:121 | ||||
| chr19:40750472-40750685 | Common:2; Rare:60 |