chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109942974399429744CT17GENIChomozygous116701626
109943041699430417CT18GENIChomozygous116701628
109943046299430463GA18GENIChomozygous116701630
109943046399430464GA17GENIChomozygous116701632
109943152199431522TC13GENIChomozygous116907231
109943181399431814CA9GENIChomozygous116907232
109943240399432403CTC20GENIChomozygous128852269
109943251399432514TC18GENIChomozygous116701646
109943308999433090TA13GENIChomozygous116907233
109943361399433613AT10GENIChomozygous131709985
109943388099433881CA19GENIChomozygous116907234
109943398699433986C15GENIChomozygous131709986
109943458699434587GA13GENIChomozygous116907235
109943483799434838GC14GENIChomozygous116907236
109943554099435541CT14GENIChomozygous116907239
109943493699434937CT11GENIChomozygous116907237
109943510999435110TC14GENIChomozygous116701650
109943531399435314AT18GENIChomozygous116907238
109943572899435728GA16GENIChomozygous131709987
109943577399435774CT16GENIChomozygous116907240
109943585799435858CT12GENIChomozygous116907241
109943628599436285TT10GENIChomozygous131709988
109943629299436292CT10GENIChomozygous131709989
109943633799436342TTTGT10GENIChomozygous131709990
109943731099437310TTTC13GENIChomozygous131709991
109943734199437342AG11GENIChomozygous116907242
109943739099437391TC17GENIChomozygous116907243
109943890399438904AG21GENIChomozygous116701652
109943900199439002GA15GENIChomozygous116701654
109943909199439092GA19GENIChomozygous116701656
109943914299439143TC24GENIChomozygous116701658
109944067099440671CT16GENIChomozygous116907244
109944099499440995AG19GENIChomozygous116701660
109944159899441599A16GENIChomozygous131709992