chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87727310777273108TC15GENIChomozygous116970380
87727545377275454TC21GENIChomozygous116970383
87727886177278862CT13GENIChomozygous116970384
87727930177279302TG23GENIChomozygous116970385
87728273277282733AG14GENIChomozygous116970386
87728296877282969TC16GENIChomozygous116970387
87728696077286961GA23GENIChomozygous116970388
87728769577287696TC29GENIChomozygous116970389
87728781577287816CA21GENIChomozygous116522984
87728827277288273AG27GENICpossibly homozygous116970390
87728883777288838GC26GENIChomozygous116970391
87729043877290439GA35GENIChomozygous116970392
87729187477291875GA30GENIChomozygous116970393
87729197877291979GA22GENIChomozygous116970394
87729416077294161CG18GENIChomozygous116970400
87729530677295307CA26GENIChomozygous116970402
87729927277299273CG35GENIChomozygous116970404
87730046577300466CT22GENIChomozygous116970405
87730368377303684AG25GENIChomozygous116970406
87731331977313320GA21GENIChomozygous116970407
87731680177316802CT18GENIChomozygous116970409
87731690377316904AG29GENIChomozygous116970410
87732090577320906TC14GENIChomozygous116970411
87732652777326528CT22GENIChomozygous116970412
87732975777329758CT20GENIChomozygous116970413
87733369877333699AG21GENIChomozygous116970414
87734270577342706GT29GENICpossibly homozygous116970416
87735160077351601AG22GENIChomozygous116522992
87735160677351607GA21GENIChomozygous117163454
87735160877351609CG21GENIChomozygous117910891
87735162077351621CG20GENIChomozygous117163456
87735162177351622TC20GENIChomozygous117910892
87735275877352759TC20GENIChomozygous116522994
87739157377391574AG22GENIChomozygous117910893
87739160277391603AG17GENIChomozygous116522996
87739161477391615AG13GENIChomozygous116844479
87739161577391616GC13GENIChomozygous116844480
87739162677391627GT15GENIChomozygous117144934
87739162877391629AG15GENIChomozygous116844481