chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X157102280157102281T13GENICheterozygous129804260
X157109747157109748AG12GENICheterozygous133046284
X157110314157110315CT14GENICheterozygous133657179
X157109764157109765CT11GENICheterozygous129832316
X157109857157109858AG13GENICheterozygous129832317
X157109878157109879AC12GENICheterozygous130204069
X157110369157110370CT19GENICheterozygous133046285
X157110384157110385GT18GENICheterozygous133046286
X157110397157110398TC18GENICheterozygous120038257
X157110406157110407TG19GENICheterozygous120038258
X157110413157110414GA21GENICheterozygous120771055
X157110426157110427AG20GENICheterozygous120038259
X157110832157110833GA12GENICheterozygous130204071
X157110839157110840AG14GENICheterozygous130204072
X157110888157110889CA10GENICheterozygous130204073
X157110898157110899CA11GENICheterozygous130204074
X157110901157110902GA11GENICheterozygous130204075
X157110906157110907GA12GENICheterozygous130204076
X157113960157113961G3GENIChomozygous133357355
X157110887157110887G10GENICheterozygous130196651