chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107413747074137471CG19GENIChomozygous68063890
107413748074137481AG18GENIChomozygous68063894
107413850874138509AG37GENIChomozygous68063898
107413995574139956GC21GENIChomozygous68063901
107414187274141873AG49GENIChomozygous68063905
107414374674143747AG40GENIChomozygous68063909
107414526674145267GC39GENIChomozygous68063912
107414561674145617AT18GENIChomozygous68063916
107414658774146588CT46GENIChomozygous68063920
107414680374146804AG36GENIChomozygous68063924
107415032874150329AC63GENIChomozygous68063928
107415086674150867CT50GENIChomozygous68063932
107415117174151172GT38GENIChomozygous68063936
107415167374151674CA46GENIChomozygous68063943
107415184474151845TA29GENIChomozygous68063946
107415316274153163GA60GENICpossibly homozygous68063949
107415407674154077CT59GENIChomozygous68063953
107415474774154748CA31GENICpossibly homozygous68063957
107415498974154990TC53GENIChomozygous68063961
107415516874155169TC54GENIChomozygous68063965
107415572274155723TC29GENIChomozygous68063969
107415591674155917GA36GENIChomozygous68063973
107415783974157840TC57GENIChomozygous68063977
107415794674157947GA50GENIChomozygous68063980
107415934674159347GT36GENIChomozygous68063984
107416476774164768CG37GENIChomozygous69192305
107416477174164772CG39GENIChomozygous68063988