chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1638174873817488TG12GENIChomozygous112197961
1638175473817548GA11GENICpossibly homozygous112197963
1638175883817589GA11GENICpossibly homozygous112197965
1638177053817706TG10GENIChomozygous112197967
1638177823817783CT11GENIChomozygous112197969
1638180163818016GGGGGGGGGC2GENIChomozygous133029193
1638180963818219CTCGGAGGGATTTCTTTTTTTTTTTTTTTTTTTTTTCTATTCTTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAGCC3GENIChomozygous133029194
1638185163818517CT21GENIChomozygous112197971
1638190163819017AC26GENIChomozygous112197973
1638194233819424GA28GENIChomozygous112197975
1638197373819738AG24GENIChomozygous112197977
1638197483819749TC26GENIChomozygous112197979
1638197573819758TC26GENIChomozygous112197981
1638197943819795GA26GENIChomozygous112197983
1638198563819857T35GENIChomozygous133029195
1638200483820049GA16GENIChomozygous112197993
1638198423819843TC32GENIChomozygous112197985
1638198593819860AC33GENIChomozygous112197987
1638199063819907TC29GENIChomozygous112197989
1638199093819910GA29GENIChomozygous112197991
1638200993820100CT18GENIChomozygous112197995
1638201183820119TA20GENIChomozygous112197997
1638201503820151TG21GENIChomozygous112197999
1638202303820231GA21GENIChomozygous112198001
1638203683820369GA20GENIChomozygous112198003
1638204633820464CT34GENIChomozygous112198005
1638206353820636TC16GENIChomozygous112198007
1638207393820740TC19GENIChomozygous112198009
1638208863820887TC20GENIChomozygous112198011