chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140756299140756300CA17GENIChomozygous61901740
1140756458140756459AT21GENIChomozygous61901741
1140756502140756503GA33GENIChomozygous61901742
1140756738140756739CG24GENIChomozygous61901743
1140756742140756743TC24GENIChomozygous61901744
1140757180140757181A-18GENIChomozygous60871250
1140757351140757352GA20GENIChomozygous61901745
1140757409140757410GA25GENIChomozygous61901746
1140757487140757488TG19GENIChomozygous61901747
1140757549140757550AT24GENIChomozygous61901748
1140757615140757616TC19GENIChomozygous61901749
1140757729140757730CT24GENIChomozygous61901750
1140757735140757736CT23GENIChomozygous61901751
1140758451140758452TA16GENIChomozygous61901752
1140758794140758795TC19GENIChomozygous61901753
1140758860140758861CCA12GENIChomozygous61901754
1140759215140759216TC24GENIChomozygous61901755
1140759424140759435AGCTTCTGGAG-----------22GENIChomozygous61901756
1140759762140759763CT19GENIChomozygous61901757
1140759973140759974TC28GENIChomozygous60871251
1140759993140759994GT28GENIChomozygous61901758
1140760129140760130AG17GENIChomozygous61901759
1140760294140760295AG17GENIChomozygous60871252
1140760522140760528CACACA------10GENICheterozygous60871254
1140760524140760528CACA----10GENICheterozygous60871255
1140760698140760699CT28GENIChomozygous61901760
1140760828140760829GA22GENIChomozygous61901761
1140760919140760920CA33GENIChomozygous61901762
1140760987140760988GC27GENIChomozygous61901763
1140761272140761273TTA21GENIChomozygous61901764
1140761329140761330TC29GENIChomozygous61901765
1140761449140761450GA28GENIChomozygous61901766
1140761482140761483GA30GENIChomozygous61901767
1140761833140761834CA35GENIChomozygous61901768
1140760428140760429GA33GENIChomozygous62160989
1140760430140760431AG33GENIChomozygous62160991
1140760520140760528CACACACA--------10GENICheterozygous62160993