chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106718943367189434CT17GENIChomozygous51680779
106718994567189950TTTTT-----13GENICheterozygous51680781
106718994667189950TTTT----13GENICpossibly homozygous51680783
106719055967190560CT37GENIChomozygous51680785
106719071067190711AG26GENIChomozygous51680787
106719168367191766CACCATGTGATTGCTGGGAATTGAACTCAGGACCTCTGGAAGAACAGTCAGTGCTCTTAACCACTGAGCCATCTCTCCAGCGC-----------------------------------------------------------------------------------35GENICheterozygous52320456
106719205967192060GC31GENIChomozygous51680793
106719262667192627CCTTTT7GENICheterozygous52383135
106719329167193292GA31GENIChomozygous52320458
106719485867194859AG29GENIChomozygous51680803
106719496367194964GT30GENIChomozygous51680805
106719537567195376GA33GENIChomozygous51680807
106719538967195391AA--36GENIChomozygous51680809
106719542867195429GT30GENIChomozygous51680811
106719544367195444TC24GENIChomozygous51680813
106719582467195825A-28GENIChomozygous51680815
106719374367193744CCTTTTTA12GENIChomozygous53154012
106719628667196287AG24GENIChomozygous51680817
106719658467196585TC34GENIChomozygous51680819
106719660467196605GA25GENIChomozygous51680821
106719692467196925GGA18GENIChomozygous53154014
106719778467197785GA28GENIChomozygous51909457
106719809067198091AG31GENIChomozygous51680840
106719816567198166AG33GENIChomozygous51909459
106719855667198557TTG2GENIChomozygous51909461
106719860667198607GA24GENIChomozygous52197071
106719873367198734CG38GENIChomozygous52197073
106719880267198803GC28GENIChomozygous53154016
106719893567198936AT31GENIChomozygous53154018
106719948767199488AG31GENIChomozygous53154020
106720146667201467AG23GENIChomozygous51680871
106720202067202021TC36GENIChomozygous53154022
106720214067202141T-22GENIChomozygous53154024
106720298667202987GGA8GENICheterozygous52383139
106720495367204954GC23GENIChomozygous51680921
106720735267207353AG31GENIChomozygous51680947
106720748467207485GGTCTATCTATCTA4GENIChomozygous53154026