chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183021820183021821CCAA16GENICheterozygous688972417
4183022663183022664GGA18GENIChomozygous688972418
4183024349183024350TC36GENIChomozygous519022770
4183024366183024367GA35GENIChomozygous519022771
4183025504183025505GA24GENIChomozygous519022772
4183025517183025523GAGAGA------18GENIChomozygous688972419
4183025566183025567TC32GENICheterozygous519022773
4183026660183026661CT22GENIChomozygous519022774
4183027418183027420AA--15GENIChomozygous688972421
4183028012183028013TC31GENIChomozygous519022775
4183028022183028023GA32GENIChomozygous519022776
4183029418183029419GA29GENIChomozygous519022777
4183030153183030154GGTGA28GENIChomozygous688972423
4183030392183030393CT16GENIChomozygous519022778
4183030662183030663CT30GENIChomozygous519022779
4183030673183030674AG32GENIChomozygous519022780
4183030737183030738TC43GENICheterozygous519022781
4183030847183030848TC35GENICheterozygous519022782
4183032232183032233AC17GENIChomozygous519022783
4183032311183032312GT23GENIChomozygous519022784
4183032618183032619AG22GENIChomozygous519022785
4183033099183033102AAA---7GENIChomozygous688972425
4183033554183033555CT32GENIChomozygous519022786
4183033622183033623AT21GENICpossibly homozygous515747997
4183034298183034300CA--7GENIChomozygous688972426
4183036184183036185TC21GENIChomozygous519022787
4183036319183036333GTGTGTGTGTGTGT--------------1GENIChomozygous688972427
4183036708183036709TC14GENIChomozygous519022788
4183037103183037104GT20GENIChomozygous515747998
4183037269183037270GA21GENIChomozygous519022789
4183037794183037795TC21GENIChomozygous519022790
4183037949183037950TG21GENIChomozygous515747999
4183038145183038146GA19GENIChomozygous519022791
4183039836183039837TA33GENIChomozygous515748000
4183040348183040349CT30GENIChomozygous519022792