chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3139688648139688649CT8GENIChomozygous670293038
3139688834139688835TG15GENIChomozygous670293039
3139688855139688856G-1GENIChomozygous768695840
3139688857139688858CA2GENIChomozygous670293040
3139688875139688876T-6GENIChomozygous768695841
3139688879139688880CA10GENICpossibly homozygous670293041
3139688880139688881AC11GENICheterozygous670293042
3139689319139689320GC12GENICheterozygous670293043
3139690392139690393AT4GENICheterozygous670293044
3139690704139690705GT17GENICpossibly homozygous670293045
3139692878139692879GA1GENIChomozygous670293046
3139693174139693175GA12GENIChomozygous670293047
3139696165139696166CA18GENICpossibly homozygous670293048
3139696829139696830TC22GENIChomozygous670293049
3139696931139696932GA28GENIChomozygous670293050
3139697162139697163GA9GENIChomozygous670293051
3139697169139697170CT6GENIChomozygous670293052
3139697918139697919CT20GENIChomozygous670293053
3139698615139698618GTG---4GENIChomozygous768695842
3139702538139702539CT5GENIChomozygous670293054
3139702547139702548CA7GENICpossibly homozygous670293055
3139703050139703051AT7GENICheterozygous670293056
3139704057139704058GA6GENICheterozygous670293057
3139704175139704176AACGTGATTGGCAGCCACTGGAGTTC7GENIChomozygous768695843
3139704343139704344TTA2GENIChomozygous768695844
3139710420139710421C-2GENICheterozygous768695845
3139710788139710789CT19GENICheterozygous670293058
3139711496139711497CA14GENICpossibly homozygous670293059
3139711619139711620AG14GENIChomozygous670293060
3139713149139713150AG29GENIChomozygous670293061