chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2143657926143657926TT41GENIChomozygous132945178
2143658933143658933T41GENIChomozygous132945179
2143662399143662400T52GENIChomozygous132945180
2143662526143662527TA39GENIChomozygous110891032
2143662548143662549GA39GENIChomozygous110891033
2143663300143663301GA43GENIChomozygous110891034
2143665414143665415GT39GENIChomozygous110891035
2143669135143669136G37GENIChomozygous132945181
2143670039143670040A40GENIChomozygous132945182
2143670815143670816T42GENICpossibly homozygous132945183
2143670951143670952TG44GENIChomozygous110891037
2143671442143671443AG56GENIChomozygous110891038
2143672641143672642CG37GENIChomozygous110891039
2143674159143674160T42GENIChomozygous132945184
2143675389143675390GC47GENIChomozygous110891040
2143676203143676204C51GENIChomozygous132945185
2143676674143676674CT44GENIChomozygous132945186
2143676793143676797AATA36GENIChomozygous132945187
2143678677143678678TA55GENIChomozygous110891041
2143678798143678799A40GENIChomozygous132945188
2143679152143679153TC38GENIChomozygous110891042
2143679388143679389TC48GENIChomozygous110891043
2143679398143679399TG44GENIChomozygous110891044
2143679441143679442GA45GENIChomozygous110891045
2143679523143679524TG36GENIChomozygous110891046
2143683618143683619TC44GENIChomozygous110891047
2143684107143684107AAT37GENIChomozygous132945189
2143684648143684649AT12GENICpossibly homozygous132948861
2143684011143684012TC22GENIChomozygous110891048
2143684640143684641AT12GENIChomozygous132948857
2143684642143684643AT12GENIChomozygous132948858
2143684644143684645AT12GENIChomozygous132948859
2143684646143684647AT12GENIChomozygous132948860
2143683950143683954GTGG13GENICheterozygous134664949
2143687230143687231AG46GENIChomozygous110891049
2143687823143687824CT40GENIChomozygous110891050
2143687880143687881GA51GENIChomozygous110891051