| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49487258-49487681 | Common:5; Rare:160 | ||||
| chr19:49489729-49489967 | Common:1; Rare:86 | ||||
| chr19:49496221-49496502 | Common:1; Rare:110 | ||||
| chr19:49527702-49528031 | Common:4; Rare:95 | ||||
| chr19:49580536-49580620 | Rare:28 | ||||
| chr19:49641826-49642087 | Rare:73 | ||||
| chr19:49665761-49666034 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49813186-49813339 | Rare:60 | ||||
| chr19:49867521-49867646 | Common:2; Rare:40; Clinvar:1 | ||||
| chr19:49877299-49877717 | Common:1; Rare:106 | ||||
| chr19:49929451-49929820 | Common:7; Rare:128 | ||||
| chr19:49929918-49930219 | Common:1; Rare:72 | ||||
| chr19:50025325-50025722 | Common:7; Rare:132 | ||||
| chr19:50384272-50384381 | Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476427-50476542 | Rare:49 |