chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125746090125746091CT21GENIChomozygous547373315
7125747342125747343CT15GENIChomozygous547373316
7125747534125747535CT21GENICpossibly homozygous547373317
7125747571125747572GA8GENICheterozygous547373318
7125748329125748330AG16GENIChomozygous547373319
7125748927125748928GA25GENICpossibly homozygous547373320
7125749012125749013GA24GENICpossibly homozygous547373321
7125749414125749415AG11GENIChomozygous547373322
7125752000125752001TC25GENIChomozygous547373323
7125752756125752757GA15GENICpossibly homozygous547373324
7125753897125753898CT5GENICheterozygous547373325
7125753949125753950GA11GENIChomozygous547373326
7125754274125754275AG9GENICpossibly homozygous547373327
7125754320125754321CT5GENIChomozygous547373328
7125754367125754368CT12GENIChomozygous547373329
7125754379125754380GC9GENICpossibly homozygous547373330
7125755157125755158GA11GENICheterozygous547373331
7125755666125755667CT24GENICpossibly homozygous547373332
7125755703125755704CT24GENIChomozygous547373333
7125756500125756501TC18GENIChomozygous547373334
7125756849125756850AG12GENICheterozygous547373335
7125757153125757154TTA2GENICheterozygous699078414