chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6136367144136367145AT13GENIChomozygous118556380
6136367145136367146TC13GENIChomozygous115082209
6136367508136367509GA13GENIChomozygous114994881
6136367802136367803TC28GENIChomozygous114994882
6136368176136368177TG34GENIChomozygous114994885
6136368755136368756GT17GENIChomozygous114994886
6136369727136369728TC23GENIChomozygous114994888
6136369954136369955AG26GENIChomozygous114994889
6136370078136370079TC26GENIChomozygous114994890
6136370100136370101TC27GENIChomozygous114994891
6136370105136370106GA26GENIChomozygous114994892
6136370522136370523TC8GENIChomozygous114994893
6136371165136371166AG23GENIChomozygous114994896
6136371211136371212GT23GENIChomozygous114994897
6136367859136367860TG22GENIChomozygous118664670
6136368865136368866CT23GENIChomozygous118664672
6136369696136369697CT21GENIChomozygous118664674
6136370882136370883CT24GENIChomozygous118664678
6136369054136369058GTTT26GENIChomozygous128400080
6136371224136371228GTGT18GENIChomozygous128400081
6136371817136371818CT20GENICpossibly homozygous114994898
6136372055136372056TC23GENIChomozygous114994899
6136372300136372301CT29GENIChomozygous114994900
6136372602136372602AGG23GENIChomozygous128400082
6136372655136372656GA27GENIChomozygous114994901
6136372927136372928GA21GENIChomozygous114994902
6136372933136372934CT20GENIChomozygous114994903
6136372999136373000AG15GENIChomozygous114994904
6136373092136373093CT28GENIChomozygous114994905
6136374633136374634CG20GENIChomozygous115302179
6136372482136372482TG23GENICpossibly homozygous131415922
6136374491136374496AGTGT17GENIChomozygous131415923
6136380598136380599CT21GENIChomozygous114994906
6136377058136377059CT8GENIChomozygous131424495