chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64080539840805399AG11GENIChomozygous114767943
64080597440805975AG24GENIChomozygous114767947
64080624040806241AG16GENIChomozygous115374503
64080653640806537TA22GENIChomozygous114767951
64080685940806860TC18GENIChomozygous115374505
64080741740807418AC29GENIChomozygous115374507
64080924740809248TG26GENIChomozygous115374509
64081002240810023CT14GENIChomozygous115374511
64081012140810122TA7GENIChomozygous115374513
64081053940810540TC7GENIChomozygous114767959
64081054440810545AG10GENIChomozygous114767961
64081080140810802AG19GENIChomozygous114767963
64081116740811168AG29GENIChomozygous115205585
64081367440813675AG9GENICheterozygous114767965
64081442040814421CT5GENIChomozygous115205589
64081553140815532CT15GENIChomozygous114767985
64081574640815747CA11GENIChomozygous115374515
64081584740815848TC27GENIChomozygous126350165
64082404340824044AC19GENIChomozygous114767997
64082406640824067GA7GENIChomozygous114767999
64082406740824068CT7GENIChomozygous126350166
64082414140824142AG13GENIChomozygous114768001
64082416140824162TC11GENIChomozygous114768003
64082432740824328AT11GENIChomozygous126371599
64082439440824395GT5GENIChomozygous126350167
64082439540824396TC6GENIChomozygous126350168
64082439640824397GC6GENIChomozygous126350169
64082779040827791TG14GENIChomozygous115374517
64082780940827810TC13GENIChomozygous114768015
64082863740828638TC15GENIChomozygous114768023
64082568540825686GA14GENIChomozygous126414745
64082586740825868GT20GENIChomozygous126414747