chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95338291053382911CG28GENIChomozygous52395035
95338331653383317TC10GENIChomozygous52395038
95338338853383389TC10GENIChomozygous51961900
95338340753383408CA12GENIChomozygous52395040
95338360253383603CT13GENIChomozygous52395042
95338561653385618CT--16GENICheterozygous53718474
95338636553386366A-13GENIChomozygous51961926
95338765653387657TC11GENIChomozygous52395044
95338808453388085CT13GENIChomozygous52395046
95338834453388345TC22GENIChomozygous52395048
95338849153388492AG16GENIChomozygous52217147
95338868953388690TC24GENIChomozygous51961939
95338889553388896CT13GENIChomozygous51961940
95338916753389168GC22GENIChomozygous52395050
95338944653389447GA15GENIChomozygous51961941
95338960453389605TC9GENIChomozygous51961942
95338989353389894TG16GENIChomozygous52395052
95339046753390468CT20GENIChomozygous52395054
95339050053390501CT17GENIChomozygous52395056
95339109953391100AC7GENIChomozygous52395058
95339165153391652TG15GENIChomozygous51961945
95339166653391667T-13GENIChomozygous51961946
95339207053392071CT24GENIChomozygous52395059
95339314153393142T-23GENIChomozygous52395061
95339371253393713CT17GENIChomozygous52395063
95339403653394037TC19GENIChomozygous51961954
95339583553395836CT15GENIChomozygous52217161
95339584253395843GT14GENIChomozygous52217162
95339591053395911CT9GENIChomozygous52395065
95339602653396027GA15GENIChomozygous52217165
95339607253396073CT15GENIChomozygous52217166
95339613753396138CT14GENIChomozygous52217167
95339620953396210TC12GENIChomozygous51961957
95339641453396415GA9GENIChomozygous51961958
95339704153397042AC16GENIChomozygous52217168
95339756553397566CT13GENIChomozygous52217169
95339759453397595GA17GENIChomozygous52217170
95339785653397857TA11GENIChomozygous52217171
95339832953398330AG13GENIChomozygous52395067
95339893553398936AT8GENIChomozygous52217172
95339938753399388CCT14GENIChomozygous51961963
95339967953399680TC16GENIChomozygous51961964