chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124866569448665695AG22GENIChomozygous50228640
124866594848665949GGA7GENICpossibly homozygous50343521
124866601348666014G-14GENIChomozygous50228644
124866625948666260GGA7GENICheterozygous50546419
124866641048666411TC7GENIChomozygous50228646
124866646148666462TG4GENIChomozygous50228648
124866647948666481AT--2GENIChomozygous50228650
124866669348666698TCCCC-----2GENIChomozygous50546420
124866670348666704AC2GENIChomozygous50228672
124866671148666712TC2GENIChomozygous50546421
124866672048666721GGGCCTTGCGCTTCCTAGGTAAGTGCTCT2GENIChomozygous50546422
124866672348666724CCACTGAGCTAAATCCCTAACCCCAAAAA2GENIChomozygous50546423
124866804548668046TC18GENIChomozygous50228674
124866808048668110CCTGCGGGGCTGCGTCTTGCGGGGCTGCGT------------------------------15GENIChomozygous50228676
124866842748668428TC6GENIChomozygous50228678
124866852448668525TC6GENIChomozygous50228682
124866861948668620TG10GENIChomozygous50228684
124866887248668873AAT9GENICpossibly homozygous50228686
124866900248669003AC16GENIChomozygous50228688
124866940348669404GA13GENIChomozygous50228689
124866971448669715T-9GENIChomozygous50228693
124867023648670237GGT30GENIChomozygous50228695
124867032448670325AG20GENIChomozygous50228697
124867096448670965GGGTTT10GENIChomozygous50228699
124867104348671071TTTCTTTCTTTCTTTCTTTCTTTCTTTC----------------------------3GENIChomozygous50546424
124867131248671317AAAAC-----12GENIChomozygous50491157
124867168348671684GA6GENIChomozygous50228707
124867238848672389CT12GENIChomozygous50491159
124867255448672555AG14GENIChomozygous50228723
124867302648673031GTTTG-----9GENIChomozygous50513624
124867303448673035G-9GENICpossibly homozygous50546425
124867321948673220GC21GENIChomozygous50228735
124867322648673227CT21GENIChomozygous50228737