chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134933704249337043GA18GENICheterozygous133684722
134938231749382318C7GENICheterozygous129052227
134945411549454116T8GENIChomozygous129052228
134945413249454133CA10GENIChomozygous114338002
134943464549434646CT10GENIChomozygous114337996
134945412349454124GC10GENIChomozygous114337998
134945412549454126TC10GENIChomozygous114338000
134945413449454135G10GENIChomozygous129052229
134945413949454140TC10GENIChomozygous114338004
134945417849454179C11GENIChomozygous129052230
134945419349454194T10GENIChomozygous129052231
134945419749454198AC10GENIChomozygous114338006
134945421149454212T11GENIChomozygous129052232
134945421749454218T12GENIChomozygous129052233
134948024049480241CT14GENICheterozygous131724486
134948034749480348GC12GENICheterozygous118580361
134948049649480497GA11GENICheterozygous130692525
134948065849480659TC12GENICheterozygous129109154
134948091349480914TC30GENICheterozygous133684723
134948082449480825A18GENICheterozygous133683925
134948118449481185CA14GENICheterozygous130422378
134948129449481295CT14GENICheterozygous130587043
134948148049481481GT11GENICheterozygous133684724
134948148749481488TA10GENICheterozygous131509550
134948151749481518AT10GENICheterozygous131509552
134948152449481525AG10GENICheterozygous133684725
134948166049481661GA23GENICheterozygous132896493
134948168049481681AC21GENICheterozygous133684726
134948170549481706AT21GENICheterozygous131509554
134948220049482201AC4GENICheterozygous131724498
134948224549482246CT6GENICheterozygous131724499
134948225849482259TC6GENICheterozygous131724500
134948225949482260GA5GENICheterozygous131724501
134948226349482264GT5GENICheterozygous131724502
134949528249495282A8GENICheterozygous131919421
134951242549512427TG23GENICheterozygous130417308