chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226692101226692102TC17GENIChomozygous110276932
2226693524226693525AG23GENIChomozygous110276941
2226693556226693557TC19GENIChomozygous110276943
2226693810226693811GA23GENIChomozygous110276945
2226695267226695272AAAGA15GENICheterozygous134185572
2226695273226695282AAAGCACGG17GENICheterozygous134185573
2226695283226695284GT17GENICheterozygous134190013
2226696654226696655CG31GENIChomozygous110828977
2226699696226699697CT24GENIChomozygous110828978
2226700818226700819CA26GENIChomozygous110828980
2226702528226702529AG21GENIChomozygous110276962
2226703554226703555CG17GENIChomozygous110828982
2226704195226704196CT27GENIChomozygous110828984
2226705875226705876GA24GENICpossibly homozygous110828986
2226712216226712217AG31GENIChomozygous110828988
2226716280226716281AT23GENIChomozygous110828990
2226720375226720376TA21GENIChomozygous110828992
2226723234226723235GA28GENIChomozygous110828994
2226727956226727957GC12GENICheterozygous134190014
2226728482226728483AC23GENICheterozygous131835875
2226699208226699208A29GENIChomozygous131302329
2226713939226713939TTGG33GENIChomozygous131302330
2226731327226731328CA18GENIChomozygous110277035
2226732381226732382CT35GENIChomozygous110829000
2226734250226734251GA38GENIChomozygous110277037
2226734792226734793GT22GENIChomozygous110829002
2226734910226734911G23GENIChomozygous131302331
2226735847226735848CT18GENIChomozygous110829004
2226736264226736265AG2GENIChomozygous133389510
2226736266226736267AG2GENIChomozygous133389511
2226741628226741629GA27GENIChomozygous110829006