chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117139845571398456TC20GENIChomozygous50821818
117139951071399511CG33GENIChomozygous50821820
117140097271400973AAGAGGAGGAGGAAGAGGAG3GENIChomozygous51188277
117140235771402358GA29GENIChomozygous50961459
117140280771402808CT24GENIChomozygous50891669
117140477971404780T-26GENIChomozygous50961460
117140498371404984AG30GENIChomozygous50961461
117140632071406321TA21GENIChomozygous50821831
117140636171406362TC23GENIChomozygous50992404
117140761371407614GC17GENIChomozygous50992405
117140942071409421GT11GENIChomozygous50992406
117140947471409475T-15GENIChomozygous50992407
117140947671409477T-11GENICheterozygous50992408
117140948971409490GC11GENICpossibly homozygous50821833
117140987471409875CG12GENIChomozygous50992409
117141044771410448A-11GENICpossibly homozygous51284134
117141172471411725CT32GENIChomozygous50821836
117141315071413151AACC9GENICheterozygous50821840
117141315071413151AACCC9GENICheterozygous50961462
117141425871414259TC41GENIChomozygous50961463
117141499771414998GGTC15GENICpossibly homozygous50961464
117141528871415289CT27GENIChomozygous50961465
117141530071415301AG27GENIChomozygous50821843
117141559871415599TC36GENIChomozygous50821845
117141795971417960T-18GENIChomozygous50961467
117141821471418215CT26GENIChomozygous50891693
117141872971418730TA23GENIChomozygous50961468
117141905071419062AGATAGATAGAT------------9GENIChomozygous51188280
117141646771416473CACACA------2GENIChomozygous51313484
117140772771407728TTTG2GENICheterozygous51196810