Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48445863-48446037 | Common:1; Rare:63 | ||||
chr19:48619139-48619560 | Common:1; Rare:138 | ||||
chr19:48811003-48811126 | Rare:43 | ||||
chr19:48965357-48965916 | Common:1; Rare:197; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr19:48993266-48993575 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49085111-49085492 | Common:3; Rare:152 | ||||
chr19:49513136-49513404 | Common:1; Rare:65 | ||||
chr19:49527861-49528036 | Common:3; Rare:54 | ||||
chr19:49580534-49580679 | Rare:45 | ||||
chr19:49641906-49642240 | Rare:94 | ||||
chr19:49665813-49665931 | Rare:56; Clinvar (pathogenic):1 | ||||
chr19:49813263-49813350 | Rare:39 | ||||
chr19:49877277-49877723 | Common:1; Rare:115 | ||||
chr19:49877839-49878156 | Common:4; Rare:98 | ||||
chr19:50476409-50476547 | Rare:64 |