chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44952739649527397TC52GENIChomozygous56876402
44952745849527459TC33GENIChomozygous56876405
44952751149527512TC20GENIChomozygous56876408
44952766549527668TTT---22GENIChomozygous58463506
44952766849527669AAAGG20GENIChomozygous58463508
44952767149527672TG21GENIChomozygous56876411
44952770949527710T-28GENIChomozygous56876414
44952779849527799TC34GENIChomozygous56876417
44952824049528241CT34GENIChomozygous56876420
44952863949528640CT42GENIChomozygous56876426
44952874849528749CT31GENIChomozygous56876429
44952879049528791CT26GENIChomozygous56876431
44952948249529483GA26GENIChomozygous56876434
44952949949529500CT33GENIChomozygous56876437
44952970349529704TC29GENIChomozygous56876440
44953039949530400CCTT19GENIChomozygous56876443
44953045249530453TG31GENIChomozygous56876446
44953045649530457TA35GENIChomozygous56876449
44953047449530475CT33GENIChomozygous56876452
44953053049530531GGA19GENIChomozygous56876455
44953071549530716AG38GENIChomozygous56876458
44953082349530824GGAA15GENIChomozygous56876461
44953100349531004AACTGTTTAATGT18GENIChomozygous56876464