chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125743757125743758G-25GENICheterozygous763292038
7125746090125746091CT31GENIChomozygous660445602
7125747342125747343CT41GENIChomozygous660445603
7125747534125747535CT37GENIChomozygous660445604
7125747571125747572GA59GENIChomozygous660445605
7125748329125748330AG41GENIChomozygous660445606
7125748832125748833C-1GENIChomozygous763292039
7125748927125748928GA35GENIChomozygous660445607
7125749012125749013GA43GENIChomozygous660445608
7125749414125749415AG12GENIChomozygous660445609
7125751521125751522AAT21GENICheterozygous763292040
7125751521125751522AATT21GENICheterozygous763292041
7125752000125752001TC24GENIChomozygous660445610
7125752756125752757GA28GENIChomozygous660445611
7125753821125753822CT38GENICheterozygous660445612
7125753869125753880TCCTTTCTCTT-----------39GENICheterozygous763292042
7125753897125753898CT35GENICpossibly homozygous660445613
7125753949125753950GA28GENIChomozygous660445614
7125754274125754275AG24GENIChomozygous660445615
7125754320125754321CT22GENIChomozygous660445616
7125754367125754368CT33GENIChomozygous660445617
7125754379125754380GC31GENIChomozygous660445618
7125755157125755158GA88GENIChomozygous660445619
7125755666125755667CT61GENIChomozygous660445620
7125755703125755704CT68GENIChomozygous660445621
7125756500125756501TC69GENIChomozygous660445622
7125756849125756850AG27GENIChomozygous660445623
7125756965125756966GGAAAA4GENIChomozygous763292044
7125757153125757154TTA9GENIChomozygous763292046