chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102640255926402560GC22GENIChomozygous516593837
102640261126402612CT22GENIChomozygous516593838
102640292126402922AAT9GENIChomozygous689476789
102640309326403094TG19GENIChomozygous516593839
102640313226403133TC16GENIChomozygous516593840
102640317126403172TTCAGCTACTGCTCATTG27GENIChomozygous689476790
102640379526403796GA11GENICheterozygous519370810
102640385526403859ACTT----6GENICheterozygous689476791
102640489226404893GA16GENIChomozygous516593841
102640495526404956CA13GENIChomozygous516593842
102640597626405977AC14GENIChomozygous516593843
102640742226407423AG12GENIChomozygous516593844
102640806226408063AG17GENIChomozygous516593845
102640920926409210TC12GENIChomozygous516593846
102640926826409269GT24GENICheterozygous519370811
102641095126410953CA--2GENIChomozygous689476792
102641504726415048CA20GENIChomozygous516593847
102641564926415650AACAAGCT5GENIChomozygous689476793
102641577026415771CG12GENICpossibly homozygous516593848
102641580026415801TC15GENICheterozygous519370812
102641580926415811TC--14GENICheterozygous689476794
102641581426415815TC17GENICheterozygous519370813
102641608926416090AATCTTT16GENIChomozygous689476795
102641647326416474CT17GENIChomozygous516593849
102641661126416612TC23GENIChomozygous516593850
102641798026417981GA12GENIChomozygous516593851
102641817926418180AG20GENIChomozygous519370814
102641847526418476GC20GENIChomozygous519370815
102641859826418604AGTAAA------11GENIChomozygous689476796
102641934326419376CAAGGGAAAGGCCAGGCTGGAGTGCCTGGTCCA---------------------------------7GENIChomozygous689476797