chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743515125743516G-33GENICheterozygous707342076
7125746090125746091CT44GENIChomozygous560705985
7125747342125747343CT25GENIChomozygous560705986
7125747534125747535CT27GENIChomozygous560705987
7125747571125747572GA36GENICpossibly homozygous560705988
7125748329125748330AG48GENIChomozygous560705989
7125748832125748833C-5GENIChomozygous707342077
7125748927125748928GA39GENIChomozygous560705990
7125749012125749013GA37GENIChomozygous560705991
7125749414125749415AG20GENIChomozygous560705992
7125751521125751522AAT10GENICheterozygous707342078
7125751521125751522AATT10GENICheterozygous707342079
7125752000125752001TC31GENIChomozygous560705993
7125752756125752757GA28GENIChomozygous560705994
7125753821125753822CT36GENIChomozygous561209805
7125753897125753898CT21GENIChomozygous560705995
7125753949125753950GA32GENIChomozygous560705996
7125754274125754275AG26GENIChomozygous560705997
7125754320125754321CT29GENIChomozygous560705998
7125754367125754368CT38GENIChomozygous560705999
7125754379125754380GC38GENIChomozygous560706000
7125755157125755158GA33GENIChomozygous560706001
7125755666125755667CT32GENIChomozygous560706002
7125755703125755704CT34GENIChomozygous560706003
7125756500125756501TC26GENIChomozygous560706004
7125756849125756850AG14GENIChomozygous560706005
7125756965125756966GGAAAA3GENIChomozygous707342081
7125757153125757154TTA13GENIChomozygous707342083