chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159406057159406058AG52GENIChomozygous55813109
5159407398159407399AAAACAAAAAAC2GENIChomozygous57292668
5159407413159407414CA4GENIChomozygous57292671
5159408147159408148AAG51GENIChomozygous55813113
5159408592159408593AAGAGATGCATAAATCCTTAAAATGCAGCTGAAAGTTGGCAATAGAGAAAAT32GENICheterozygous57590868
5159409345159409346TC84GENICpossibly homozygous55813129
5159409644159409645TC42GENIChomozygous55813131
5159409775159409788ACAGGCAAGGCAC-------------45GENIChomozygous57292674
5159410158159410159AG61GENIChomozygous57292677
5159410573159410574TC58GENIChomozygous57292680
5159411315159411316GA46GENIChomozygous57292683
5159412643159412651GATGGATG--------25GENIChomozygous57292686
5159412685159412686TC51GENICpossibly homozygous55813149
5159412709159412710CCGGAT52GENICpossibly homozygous55813154
5159413214159413215GT40GENIChomozygous57292689
5159410997159411000GGT---13GENICheterozygous56358322
5159413636159413637GA38GENIChomozygous57292692
5159413879159413880CCA24GENIChomozygous57292695
5159414749159414750GA41GENIChomozygous57292698
5159416084159416085AG32GENIChomozygous55813164
5159416265159416275AGAGCACTCC----------39GENIChomozygous57292701
5159417352159417353TC97GENIChomozygous55813166
5159418133159418134CT31GENIChomozygous57292704
5159418823159418825CC--17GENIChomozygous56358330
5159419035159419036AG56GENIChomozygous56358332
5159419058159419059GA62GENIChomozygous56358334
5159419360159419361CT2GENIChomozygous57292707
5159419603159419604GA58GENIChomozygous57292710
5159419957159419958TC51GENIChomozygous56358335
5159422132159422133TC67GENIChomozygous55813173
5159422266159422267TG54GENIChomozygous55813175
5159422382159422383AG50GENICpossibly homozygous55813177
5159422834159422835GA61GENIChomozygous55813179
5159424007159424008TC50GENIChomozygous55813181
5159424628159424629TA11GENIChomozygous55813183