chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118327324118327325TG11GENIChomozygous55050792
6118330368118330369T-3GENIChomozygous54961157
6118330477118330478GC9GENIChomozygous55265097
6118337412118337414AC--2GENICheterozygous55265100
6118343111118343119GGGGGGGG--------8GENICheterozygous54961229
6118346141118346142GA13GENICheterozygous55265111
6118346703118346704AATTTCTTT2GENIChomozygous55428860
6118351692118351693G-6GENIChomozygous54667284
6118351693118351694CA6GENIChomozygous55428862
6118351735118351736GT4GENIChomozygous54667288
6118351741118351742TG4GENIChomozygous54667290
6118351744118351745CA3GENIChomozygous54667292
6118351759118351760AG5GENIChomozygous54667294
6118352294118352295TC14GENICpossibly homozygous54961247
6118352521118352522CT16GENIChomozygous55265125
6118352731118352732GGAGA8GENICpossibly homozygous54667296
6118352799118352800A-7GENICpossibly homozygous55265128
6118352834118352835CA13GENIChomozygous55265131
6118353640118353641CT13GENIChomozygous55265135
6118353656118353657GA13GENIChomozygous55265138
6118355059118355060CA18GENIChomozygous54961249
6118355157118355158TC9GENIChomozygous55265141
6118355877118355879AC--2GENIChomozygous55265146
6118356593118356594CT15GENIChomozygous55265152
6118356686118356687AAT7GENICheterozygous55265155
6118357799118357800GA12GENIChomozygous55265158
6118360328118360329CT12GENIChomozygous55265161
6118361133118361134CT10GENIChomozygous55265164
6118363663118363664CA7GENICpossibly homozygous55265167
6118366191118366192GGGAA3GENIChomozygous54961269
6118366334118366335GT12GENIChomozygous55265170
6118368243118368244AAC1GENIChomozygous54667312
6118368247118368248C-1GENIChomozygous54667314
6118368265118368266TC2GENIChomozygous54667316
6118368271118368272GGT2GENIChomozygous54667318
6118370002118370003AG17GENIChomozygous55265173
6118371185118371186AG9GENIChomozygous55265178
6118371923118371924CA8GENIChomozygous55265181
6118372037118372038CT15GENICpossibly homozygous55265184
6118372633118372634AC6GENIChomozygous55265187