chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104497795544977956GT15GENIChomozygous51441478
104497819144978192CT14GENICpossibly homozygous51441480
104497850544978506CA20GENICpossibly homozygous51441483
104498004444980045TC18GENICpossibly homozygous52051794
104497921944979220T-4GENIChomozygous52051792
104498065444980655TC22GENIChomozygous52051796
104498165244981653TC11GENIChomozygous52051798
104498188044981881CT13GENIChomozygous52051800
104498190144981902T-14GENIChomozygous51441486
104498204544982046GA9GENIChomozygous52051802
104498246644982467A-4GENIChomozygous52051804
104498330344983304AG17GENIChomozygous52051806
104498331644983317AG15GENIChomozygous52051808
104498440744984408GA12GENIChomozygous52051834
104498446144984462CA8GENIChomozygous52051836
104498622144986222C-9GENICheterozygous52051854
104498692544986926GA2GENIChomozygous52051860
104499008544990086GA11GENICpossibly homozygous51872671
104499072544990726AG6GENICheterozygous52051876
104499147344991474TC7GENIChomozygous52051880
104499150244991503CG12GENICpossibly homozygous52051882
104499182144991822AC4GENIChomozygous52051886
104499199944992000AC4GENIChomozygous52051890
104499230344992304CT11GENIChomozygous52051892
104499233544992336TC17GENIChomozygous51441536
104499237344992374AG22GENIChomozygous51635827
104499261344992614TC13GENICheterozygous52051894
104499271044992711TC5GENICheterozygous52051896
104499271844992719TC3GENIChomozygous52051898
104499289144992892CCAAA1GENIChomozygous51441537
104499332544993326GA20GENIChomozygous52051902
104499335144993352GA15GENICpossibly homozygous52051904
104499337144993372AAGAG3GENICheterozygous51441539
104499338944993390GA5GENICheterozygous52051906
104499340444993405G-9GENIChomozygous52051908
104499376044993761GA4GENIChomozygous52051912
104499381044993811GT6GENICheterozygous52051914
104499389744993898CT6GENICheterozygous52051916
104499402744994028CT7GENICpossibly homozygous52051918
104499405344994054A-6GENIChomozygous52051920
104499407244994073TA14GENICpossibly homozygous52051922
104499415344994154CT18GENICpossibly homozygous52051924
104499439144994392AG24GENICpossibly homozygous52051926
104499443544994439CACA----12GENICheterozygous52051928
104499464544994646AC29GENICpossibly homozygous52051934
104499483044994831AAG3GENIChomozygous52051936
104499483244994835TAT---3GENIChomozygous52051938
104499496244994963AG17GENIChomozygous52051942
104499526444995265CT13GENIChomozygous52051944
104499600344996004GGA5GENIChomozygous52051950
104499650844996509CCCTGT4GENIChomozygous51441548
104499654144996542AG15GENIChomozygous51635829
104499745344997454AT8GENIChomozygous52051956
104499758344997584CA14GENICpossibly homozygous52051958
104499762244997623AG2GENIChomozygous51441550
104499780344997804CG6GENIChomozygous52051964
104499818744998188TTA3GENIChomozygous51441552
104499823344998234CG11GENIChomozygous52051966
104499885744998858CT24GENICheterozygous52051968
104499898744998988CT19GENICpossibly homozygous52051970
104499918144999182TC18GENIChomozygous51441553
104499921244999213TC19GENIChomozygous52051972
104499925744999258TC16GENICpossibly homozygous52051974
104499927244999273CG24GENICpossibly homozygous52051976
104499941444999415CT25GENICpossibly homozygous52051978
104499959744999598TC19GENIChomozygous52051980
104499970444999705TC19GENICpossibly homozygous52051982
104499972244999723GA17GENIChomozygous52051984
104499986144999862TC12GENIChomozygous51441554
104500000345000004TG11GENIChomozygous52051986
104500001545000016TC7GENIChomozygous52051988
104500001645000017TG8GENIChomozygous52051990