chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44952739649527397TC24GENIChomozygous56876402
44952745849527459TC26GENIChomozygous56876405
44952751149527512TC28GENICpossibly homozygous56876408
44952766549527668TTT---22GENIChomozygous58463506
44952766849527669AAAGG21GENIChomozygous58463508
44952767149527672TG20GENIChomozygous56876411
44952770949527710T-23GENIChomozygous56876414
44952779849527799TC36GENIChomozygous56876417
44952824049528241CT10GENIChomozygous56876420
44952863949528640CT14GENIChomozygous56876426
44952874849528749CT22GENIChomozygous56876429
44952879049528791CT15GENIChomozygous56876431
44952948249529483GA21GENIChomozygous56876434
44952949949529500CT21GENIChomozygous56876437
44952970349529704TC18GENIChomozygous56876440
44953039949530400CCTT18GENICpossibly homozygous56876443
44953045249530453TG24GENIChomozygous56876446
44953045649530457TA24GENIChomozygous56876449
44953047449530475CT25GENIChomozygous56876452
44953053049530531GGA10GENIChomozygous56876455
44953071549530716AG20GENIChomozygous56876458
44953082349530824GGAA21GENIChomozygous56876461
44953100349531004AACTGTTTAATGT31GENIChomozygous56876464