chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135723731357237314TG17GENICheterozygous51286427
135723731457237315GT17GENICheterozygous51286429
135723731657237317GT17GENICheterozygous51286431
135723731757237318TC17GENICheterozygous51286433
135731484557314846CG13GENICheterozygous49955564
135732309257323093TC10GENICheterozygous49955581
135732639057326391TC21GENICheterozygous49955593
135732653957326540TC24GENICheterozygous49955594
135734697557346976CT11GENICheterozygous50232222
135734868657348687CT22GENICheterozygous50232226
135736485857364859GA26GENICheterozygous49955709
135736500957365010CT13GENICheterozygous50232242
135736501157365012CT13GENICheterozygous50232244
135736501257365013AG13GENICheterozygous50232246
135737223157372232CT18GENICheterozygous50232252
135737608057376081CT30GENICheterozygous49955744
135738757557387576CT7GENICheterozygous49955780
135738794357387944AG10GENICheterozygous49955781
135738797657387977AT7GENICheterozygous49955782
135738981057389811TC19GENICheterozygous49955790
135743640457436405TA21GENICheterozygous49955961
135744373157443732AG24GENICheterozygous49955978
135746350257463503GA13GENICheterozygous50232406
135747833257478333AG32GENICheterozygous49956080
135748518957485190CT16GENICheterozygous50232480
135750051857500519AC19GENICheterozygous50232570
135751415557514156CT6GENICheterozygous50232640