chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4222126305222126306CT10GENIChomozygous57101915
4222128014222128015AG22GENIChomozygous57101916
4222128018222128019GA22GENIChomozygous57101917
4222129368222129369CCGTATGTGTGTGT17GENICheterozygous58375245
4222130021222130022AG27GENIChomozygous57101918
4222130290222130292AA--4GENICheterozygous57101919
4222130291222130292A-4GENICheterozygous57101920
4222131066222131070TGTA----3GENICheterozygous58609044
4222135371222135373TT--10GENICheterozygous58375247
4222135372222135373T-10GENICheterozygous58375249
4222135429222135430AG17GENIChomozygous57101942
4222135477222135478AT20GENIChomozygous57101943
4222137550222137551TC34GENIChomozygous57101944
4222137601222137602CCGA30GENIChomozygous57101945
4222137749222137750TG21GENIChomozygous57101946
4222137752222137753CA22GENIChomozygous57101947
4222137997222137998CCT15GENICheterozygous57644636
4222138066222138067CT25GENIChomozygous57101948
4222140220222140224ACAC----14GENICpossibly homozygous58375251
4222141192222141193AT22GENIChomozygous57101950