chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA45GENIChomozygous797255597
1263813164263813165CA24GENIChomozygous797255598
1263813492263813493TA35GENIChomozygous797255599
1263814011263814012CT35GENIChomozygous797255600
1263814051263814052CT43GENICpossibly homozygous797255601
1263814338263814339GA29GENIChomozygous797255602
1263815026263815027CT21GENIChomozygous797255603
1263815349263815350GA20GENIChomozygous797255604
1263815744263815745AG24GENIChomozygous797255605
1263817320263817321GA16GENIChomozygous797255606
1263817743263817744AG30GENIChomozygous797255607
1263818715263818716GA23GENIChomozygous797255608
1263819181263819182CT33GENIChomozygous797255609
1263820712263820713TC27GENIChomozygous797255610
1263820813263820814AG26GENIChomozygous797255611
1263820861263820862CT28GENIChomozygous797255612
1263823243263823244CT34GENIChomozygous797255613
1263825226263825227CT40GENICheterozygous797255614
1263825765263825766GT27GENIChomozygous797255615
1263826119263826120GA28GENIChomozygous797255616
1263827331263827332GA20GENIChomozygous797255617
1263828502263828503CA23GENIChomozygous797255618
1263830697263830698GA21GENIChomozygous797255619
1263831722263831723CT27GENIChomozygous797255620
1263832813263832814AG25GENIChomozygous797255621
1263835278263835279CT32GENIChomozygous797255622
1263835926263835927GA15GENIChomozygous797255623
1263840399263840400GA14GENIChomozygous797255624
1263843300263843301AT29GENIChomozygous797255625