chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135723731357237314TG20GENICheterozygous51286427
135723731457237315GT20GENICheterozygous51286429
135723731657237317GT20GENICheterozygous51286431
135723731757237318TC20GENICheterozygous51286433
135731484557314846CG17GENICheterozygous49955564
135732309257323093TC9GENICheterozygous49955581
135732639057326391TC16GENICheterozygous49955593
135732653957326540TC24GENICheterozygous49955594
135734697557346976CT17GENICheterozygous50232222
135734868657348687CT26GENICheterozygous50232226
135736485857364859GA25GENICheterozygous49955709
135736500957365010CT22GENICheterozygous50232242
135736501157365012CT22GENICheterozygous50232244
135736501257365013AG22GENICheterozygous50232246
135737223157372232CT23GENICheterozygous50232252
135737608057376081CT38GENICheterozygous49955744
135737710357377104AG5GENICheterozygous49955749
135738757557387576CT12GENICheterozygous49955780
135738794357387944AG5GENICheterozygous49955781
135738981057389811TC21GENICheterozygous49955790
135742287357422874TC8GENICheterozygous49955908
135743640457436405TA34GENICheterozygous49955961
135743643557436436AG31GENICheterozygous49955962
135744373157443732AG21GENICheterozygous49955978
135746350257463503GA14GENICheterozygous50232406
135747833257478333AG18GENICheterozygous49956080
135748518957485190CT16GENICheterozygous50232480
135750051857500519AC18GENICheterozygous50232570
135751415557514156CT7GENICheterozygous50232640