chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142193029142193030AG5GENIChomozygous56960150
4142195064142195065CT9GENIChomozygous56960159
4142196339142196343AAAA----2GENIChomozygous58589436
4142197968142197969AG20GENIChomozygous56960164
4142198973142198974CA11GENIChomozygous56960169
4142199365142199366GA13GENIChomozygous56960170
4142201631142201632GA10GENICpossibly homozygous56960179
4142201650142201651A-7GENIChomozygous58589438
4142202130142202131TA11GENICpossibly homozygous56960181
4142202198142202199GT13GENIChomozygous56960182
4142202612142202613GA16GENIChomozygous58589440
4142203716142203717CCAG5GENIChomozygous56960184
4142204031142204032T-10GENIChomozygous56960186
4142204410142204411AT14GENIChomozygous56960187
4142204921142204922TA3GENIChomozygous56960188
4142201909142202031AGAAATTGTGGCACTGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGACCCAAAAAAAAAAAAAAAAAAA--------------------------------------------------------------------------------------------------------------------------7GENICpossibly homozygous58283692
4142204033142204034CA10GENIChomozygous58283694
4142206160142206161CT13GENICheterozygous58589442
4142206537142206541TTAC----5GENIChomozygous56960190
4142206945142206946TC16GENIChomozygous56960192
4142207106142207107AG15GENICpossibly homozygous56960193
4142207410142207411A-1GENIChomozygous58589444
4142207711142207712GA11GENICheterozygous58589446
4142209069142209070AG5GENIChomozygous57342156
4142209070142209071TA5GENIChomozygous57342158
4142209439142209440AG17GENIChomozygous56960194
4142210145142210147CA--1GENIChomozygous56960196
4142211418142211419TC14GENIChomozygous56960197
4142211536142211537TTGTTTCA3GENIChomozygous56960198