Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49641826-49642081 | Rare:70 | ||||
chr19:49665577-49666027 | Common:6; Rare:207; Clinvar (pathogenic):1 | ||||
chr19:49690980-49691142 | Rare:36 | ||||
chr19:49808775-49809001 | Common:2; Rare:73 | ||||
chr19:49813181-49813350 | Rare:70 | ||||
chr19:49850949-49851173 | Common:1; Rare:89 | ||||
chr19:49854509-49854687 | Common:1; Rare:69 | ||||
chr19:49857531-49857720 | Common:2; Rare:68 | ||||
chr19:49867205-49867368 | Common:1; Rare:56; Clinvar (benign):5 | ||||
chr19:49867468-49867643 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):5 | ||||
chr19:49877271-49877743 | Common:2; Rare:126 | ||||
chr19:49877835-49878136 | Common:5; Rare:94 | ||||
chr19:49929111-49929225 | Common:3; Rare:35 | ||||
chr19:49929408-49929757 | Common:7; Rare:119 | ||||
chr19:49929922-49930208 | Common:1; Rare:67 |