chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183751484183751485TA22GENIChomozygous57986054
4183752345183752346GT2GENIChomozygous57986060
4183752349183752350T-1GENIChomozygous57986063
4183752380183752381GC13GENICheterozygous57986067
4183753094183753095GA19GENICpossibly homozygous57986070
4183753460183753461TTTGTTGTTGA4GENIChomozygous57986073
4183754663183754664A-13GENIChomozygous57986076
4183755461183755462TC26GENICpossibly homozygous57561676
4183755570183755571CT16GENIChomozygous57986079
4183755582183755583CA11GENIChomozygous57986082
4183756234183756235GA12GENIChomozygous57561680
4183756815183756816GA16GENICheterozygous57986085
4183756860183756861TC18GENIChomozygous57986088