chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1163318318163318319CT27GENICpossibly homozygous109339003
1163319109163319110TC23GENIChomozygous108347504
1163321370163321371A18GENIChomozygous127451785
1163322013163322014CT31GENIChomozygous108347520
1163322265163322266AG21GENIChomozygous108347522
1163322325163322326CT23GENIChomozygous108347524
1163322581163322582GA37GENIChomozygous108952403
1163323384163323385GT25GENIChomozygous108347526
1163323420163323421GC24GENIChomozygous108347528
1163324027163324028TG30GENIChomozygous108952404
1163324885163324886A18GENIChomozygous131578230
1163324888163324891TAT18GENIChomozygous131578231
1163324891163324892TC18GENIChomozygous120577453
1163325550163325551TC22GENIChomozygous108347540
1163325604163325605TC19GENIChomozygous108347542
1163325752163325753TC28GENIChomozygous108347544
1163325908163325909CT27GENIChomozygous109339005
1163325969163325970AG29GENIChomozygous109339007
1163326112163326113TA33GENIChomozygous108347546
1163326764163326764TGG30GENIChomozygous131578232
1163326793163326794CT27GENIChomozygous108347548
1163327687163327688CT33GENIChomozygous109339009
1163327704163327705CA31GENIChomozygous109161629