| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48624191-48624426 | Common:1; Rare:69 | ||||
| chr19:48872237-48872449 | Common:2; Rare:75 | ||||
| chr19:48900197-48900367 | Common:1; Rare:60 | ||||
| chr19:48933485-48933696 | Common:3; Rare:54 | ||||
| chr19:48955185-48955340 | Common:1; Rare:33 | ||||
| chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993253-48993825 | Common:5; Rare:197; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085116-49085515 | Common:3; Rare:165 | ||||
| chr19:49451754-49452002 | Common:3; Rare:64 | ||||
| chr19:49453024-49453295 | Common:2; Rare:82 | ||||
| chr19:49527817-49528031 | Common:3; Rare:72 | ||||
| chr19:49580515-49580686 | Rare:58 | ||||
| chr19:49581324-49581367 | Common:1; Rare:8 | ||||
| chr19:49665744-49666029 | Common:3; Rare:137; Clinvar (pathogenic):1 | ||||
| chr19:49867499-49867620 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):2 |