chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142188873142188874TG1GENIChomozygous56960147
4142191098142191099TA20GENICpossibly homozygous56960149
4142193029142193030AG3GENIChomozygous56960150
4142193884142193892TTTTTTTT--------1GENIChomozygous56960151
4142194104142194105GA15GENICpossibly homozygous56960153
4142194384142194385CT8GENIChomozygous56960154
4142195064142195065CT11GENIChomozygous56960159
4142195590142195592GG--8GENIChomozygous56960160
4142196342142196343A-4GENICheterozygous58509697
4142196378142196388ACACACACAC----------1GENIChomozygous56960162
4142197136142197137A-2GENICheterozygous58526656
4142197968142197969AG18GENIChomozygous56960164
4142198973142198974CA13GENIChomozygous56960169
4142199365142199366GA12GENICpossibly homozygous56960170
4142201631142201632GA3GENIChomozygous56960179
4142201772142201773GA19GENICpossibly homozygous56960180
4142202130142202131TA9GENIChomozygous56960181
4142202198142202199GT8GENIChomozygous56960182
4142203101142203103AA--3GENICheterozygous56960183
4142203716142203717CCAG5GENICheterozygous56960184
4142204031142204032T-5GENIChomozygous56960186
4142204033142204034CA6GENIChomozygous58283694
4142204410142204411AT17GENIChomozygous56960187
4142204921142204922TA2GENIChomozygous56960188
4142206311142206312GA12GENIChomozygous56960189
4142206537142206541TTAC----2GENIChomozygous56960190
4142206580142206581AAT1GENIChomozygous56960191
4142206945142206946TC15GENIChomozygous56960192
4142207106142207107AG19GENIChomozygous56960193
4142209069142209070AG10GENIChomozygous57342156
4142209070142209071TA10GENIChomozygous57342158
4142209439142209440AG15GENICpossibly homozygous56960194
4142210126142210127TTAA2GENICheterozygous56960195
4142210145142210147CA--5GENICheterozygous56960196
4142211418142211419TC14GENICpossibly homozygous56960197
4142211536142211537TTGTTTCA5GENICheterozygous56960198
4142211608142211609TC21GENIChomozygous56960199
4142215166142215168GG--5GENICheterozygous56960201
4142215168142215169GA4GENIChomozygous58283696