chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214124348214124349AG38GENIChomozygous806074719
1214124388214124389CA34GENICheterozygous806074720
1214124410214124411CA36GENIChomozygous806074721
1214126166214126167TA80GENICheterozygous806074722
1214126214214126215GA117GENICheterozygous806074723
1214126263214126264TC121GENICheterozygous806074724
1214126267214126268AT113GENICheterozygous806074725
1214126557214126558GA13GENIChomozygous806074726
1214126561214126562CG12GENIChomozygous806074727
1214127053214127054GA92GENICpossibly homozygous806074728
1214127433214127434TC70GENICpossibly homozygous806074729
1214129031214129032TC54GENIChomozygous806074730
1214130226214130227GA44GENIChomozygous806074731
1214131357214131358AG40GENIChomozygous806074732
1214132380214132381AG67GENICpossibly homozygous806074733
1214132530214132531CT66GENIChomozygous806074734
1214136340214136341TG48GENICheterozygous806074735
1214137707214137708CG35GENICheterozygous806074736
1214137715214137716CG36GENICheterozygous806074737
1214138871214138872GA52GENIChomozygous806074738
1214140632214140633CT37GENIChomozygous806074739
1214140827214140828GT44GENICpossibly homozygous806074740
1214140994214140995GT51GENIChomozygous806074741
1214141343214141344AG33GENIChomozygous806074742
1214143187214143188CT51GENIChomozygous806074743
1214143347214143348AG49GENIChomozygous806074744
1214144102214144103GA43GENIChomozygous806074745
1214146027214146028TC46GENICpossibly homozygous806074746
1214147016214147017CT35GENIChomozygous806074747