chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199992840199992841TC10GENIChomozygous545792893
1199992982199992983AG1GENIChomozygous545792894
1199993355199993356GC10GENIChomozygous545792895
1199994087199994088G-15GENIChomozygous698334795
1199994128199994129A-21GENICpossibly homozygous698334796
1199994899199994900CT14GENICpossibly homozygous545792896
1199995938199995939CT19GENIChomozygous547656326
1199997901199997902TC10GENICpossibly homozygous545792897
1199999309199999310CT4GENIChomozygous545792898
1200000500200000501AG9GENIChomozygous545792899
1200000545200000546TC8GENICheterozygous545792900
1200000546200000547TC8GENICheterozygous545792901
1200001048200001049AG2GENIChomozygous545792902
1200002107200002108AT14GENICpossibly homozygous545792903
1200002177200002178TC23GENICpossibly homozygous545792904
1200002528200002529CA12GENICpossibly homozygous545792905
1200003589200003590T-11GENIChomozygous698334797
1200004527200004528GA15GENIChomozygous545792906
1200006624200006625TC9GENICpossibly homozygous545792907
1200006876200006877CT13GENICpossibly homozygous545792908
1200008107200008108CT27GENICpossibly homozygous545792909
1200008253200008254GA25GENIChomozygous545792910
1200008385200008386CA19GENIChomozygous545792911
1200008663200008664CCT14GENIChomozygous698334798
1200008815200008816T-8GENICheterozygous698334799
1200009080200009081CG15GENICpossibly homozygous545792912
1200009168200009169TTA10GENIChomozygous698334800
1200009352200009353TTGAGA2GENIChomozygous698334801
1200009777200009778GT25GENICheterozygous547656327
1200009778200009779GT25GENICheterozygous547656328
1200014895200014896T-6GENICheterozygous698334802
1200016711200016712TG9GENIChomozygous545792913
1200017254200017256AA--1GENIChomozygous698334803
1200020966200020967GA12GENICpossibly homozygous545792914
1200022798200022799CCG7GENICheterozygous698334805
1200022970200022971TC8GENIChomozygous545792915