| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48933475-48933702 | Common:3; Rare:59 | ||||
| chr19:48964971-48965275 | Common:1; Rare:63 | ||||
| chr19:48965278-48965609 | Rare:108; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993287-48993508 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:48993553-48993914 | Common:5; Rare:94 | ||||
| chr19:49085096-49085537 | Common:3; Rare:173 | ||||
| chr19:49114136-49114396 | Common:4; Rare:58 | ||||
| chr19:49155387-49155610 | Rare:39 | ||||
| chr19:49335379-49335478 | Common:1; Rare:24 | ||||
| chr19:49362375-49362490 | Rare:35 | ||||
| chr19:49453094-49453311 | Common:1; Rare:69 | ||||
| chr19:49453473-49453639 | Common:1; Rare:48 | ||||
| chr19:49489729-49489921 | Common:1; Rare:63 | ||||
| chr19:49512602-49512762 | Rare:37 | ||||
| chr19:49527864-49528034 | Common:3; Rare:52 |