chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135128462651284627AG26GENIChomozygous890476969
135128502551285026GA21GENIChomozygous890476970
135128661351286614TG8GENIChomozygous890476971
135128665151286652CT19GENIChomozygous890476972
135128727851287279GA7GENIChomozygous890476973
135128843851288439TC15GENIChomozygous890476974
135128956551289566AG21GENIChomozygous890476975
135128968151289682TC4GENIChomozygous890476976
135128968251289683TC4GENIChomozygous890476977
135129055851290559TC17GENIChomozygous890476978
135129593851295939GA9GENIChomozygous890476979
135129632051296321CT5GENIChomozygous890476980
135129698451296985GA16GENIChomozygous890476981
135129869351298694GC4GENIChomozygous890476982
135129869451298695GA4GENIChomozygous890476983
135130294751302948CT7GENIChomozygous890476984
135130311751303118GT11GENIChomozygous890476985
135130369251303693TC6GENIChomozygous890476986
135130372051303721AG12GENIChomozygous890476987
135130411551304116GA4GENIChomozygous890476988
135130654151306542CT16GENIChomozygous890476989
135130762751307628GA18GENIChomozygous890476990
135130812751308128AC9GENIChomozygous890476991
135131139551311396AG17GENIChomozygous890476992
135131169851311699CT12GENIChomozygous890476993
135131317251313173CA20GENIChomozygous890476994
135131366051313661AG15GENICheterozygous890476995