chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142190932142190933CT8GENIChomozygous57942279
4142193029142193030AG5GENIChomozygous56960150
4142195064142195065CT9GENIChomozygous56960159
4142195590142195592GG--5GENIChomozygous56960160
4142196042142196043CT14GENICpossibly homozygous57942281
4142196378142196388ACACACACAC----------3GENIChomozygous56960162
4142196571142196572CT17GENIChomozygous58777160
4142197135142197137AA--1GENIChomozygous57942284
4142197968142197969AG12GENIChomozygous56960164
4142198973142198974CA16GENICpossibly homozygous56960169
4142199365142199366GA7GENIChomozygous56960170
4142201631142201632GA14GENICpossibly homozygous56960179
4142201772142201773GA13GENIChomozygous56960180
4142202130142202131TA12GENIChomozygous56960181
4142202198142202199GT12GENICpossibly homozygous56960182
4142203101142203103AA--5GENIChomozygous56960183
4142203716142203717CCAG6GENIChomozygous56960184
4142204031142204032T-3GENIChomozygous56960186
4142204410142204411AT17GENIChomozygous56960187
4142204921142204922TA5GENICheterozygous56960188
4142206537142206541TTAC----11GENICpossibly homozygous56960190
4142206945142206946TC12GENIChomozygous56960192
4142207106142207107AG9GENIChomozygous56960193
4142209069142209070AG9GENIChomozygous57342156
4142209070142209071TA8GENIChomozygous57342158
4142209439142209440AG12GENICpossibly homozygous56960194
4142210126142210127TTAA1GENIChomozygous56960195
4142210145142210147CA--3GENICheterozygous56960196
4142211418142211419TC10GENIChomozygous56960197
4142215166142215168GG--9GENICpossibly homozygous56960201
4142215168142215169GA8GENIChomozygous58283696
4142201909142202031AGAAATTGTGGCACTGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGACCCAAAAAAAAAAAAAAAAAAA--------------------------------------------------------------------------------------------------------------------------4GENICheterozygous58283692
4142204033142204034CA3GENIChomozygous58283694