chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135128102251281023CT11GENIChomozygous114948055
135128164151281642CT17GENIChomozygous114890601
135128454951284550AG15GENIChomozygous114890603
135128502551285026GA17GENIChomozygous114762986
135128665151286652CT22GENIChomozygous114762990
135128968151289682TC19GENIChomozygous114762996
135128968251289683TC19GENIChomozygous114762998
135128981451289815GA22GENIChomozygous114890605
135128989251289893TG16GENIChomozygous114890607
135129418651294187CT9GENIChomozygous114890609
135129593851295939GA24GENIChomozygous114763002
135129869351298694GC25GENIChomozygous114763008
135129869451298695GA26GENIChomozygous114763010
135130005751300058CT12GENIChomozygous114890611
135130059651300597GA23GENIChomozygous114890613
135130369251303693TC13GENIChomozygous114763014
135130411551304116GA16GENIChomozygous114763018
135128462651284627AG13GENIChomozygous114343039
135130735651307357G4GENIChomozygous130106702
135129055851290559TC20GENIChomozygous114343041
135129461851294618TT21GENIChomozygous131126481
135130720351307203C6GENIChomozygous129053105
135130724451307246AG3GENIChomozygous129053106
135130727851307279G3GENIChomozygous129053107
135130728851307288A3GENIChomozygous129053108
135130729151307291T3GENIChomozygous129053109
135130730851307308T1GENIChomozygous129053110
135130739151307391A6GENIChomozygous129053111
135130734951307350GT4GENIChomozygous130113591