chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204375056043750561AG37GENIChomozygous63516451
204375081343750814TC21GENIChomozygous63516452
204375167443751675CT15GENIChomozygous63516453
204375180343751804AG16GENIChomozygous63516454
204375247443752475TC18GENIChomozygous63516455
204375261843752619TC20GENIChomozygous63516456
204375345343753454GT22GENIChomozygous63516457
204375348943753490AT19GENICheterozygous63516458
204375565443755655GC15GENIChomozygous63516461
204375716943757170TG14GENIChomozygous63516462
204375765843757659AG27GENIChomozygous63516463
204375787343757874TC6GENIChomozygous63516464
204375849243758493CG16GENIChomozygous63516465
204375971043759711AG15GENIChomozygous63516469
204376073543760736AC27GENIChomozygous63516470
204376090843760909GT28GENIChomozygous63516471
204377000843770009GA18GENIChomozygous63516473
204377454243774543TC15GENIChomozygous63516475
204377460343774604AC18GENICheterozygous63516476
204377761943777620CG17GENIChomozygous63516477
204377770143777702GC21GENIChomozygous63516478
204377834543778346TC20GENIChomozygous63516479
204377997143779972CA20GENICpossibly homozygous63516480
204378319443783195GA27GENIChomozygous63516482
204378320143783202CT23GENIChomozygous63516483
204378401643784017AC19GENIChomozygous63516484
204378494743784948TA27GENICpossibly homozygous63516485
204378504643785047CT23GENICheterozygous63516486
204378602943786030GA27GENIChomozygous63516488
204378637543786376GA25GENIChomozygous63516489
204378925243789253GA24GENIChomozygous63516490
204378939243789393CA17GENIChomozygous63516491
204378960043789601TA23GENIChomozygous63516492
204378987743789878TC23GENICpossibly homozygous63516493
204379038143790382AG24GENIChomozygous63516494
204379084143790842GA11GENIChomozygous63516496
204379116043791161GA19GENIChomozygous63516497
204379183943791840TC15GENIChomozygous63516499
204379189943791900CT18GENIChomozygous63516500