chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103607921836079219CT24GENIChomozygous51848958
103607934336079344AG19GENIChomozygous51411305
103607963036079631AG17GENIChomozygous51411307
103607969736079698AG24GENIChomozygous51411309
103608006636080067AG22GENIChomozygous51411313
103608011936080120GC24GENIChomozygous51411315
103608029036080291CG19GENIChomozygous51848962
103608057336080574AG20GENIChomozygous51848965
103608095936080960TC23GENIChomozygous51411321
103608497336084974AC19GENIChomozygous51411339
103608500636085007TC21GENIChomozygous51411341
103608602336086024GGCATA9GENIChomozygous51848974
103608610736086108AT16GENIChomozygous51411359
103608674436086745CT22GENIChomozygous51848976
103608869536088696TC13GENIChomozygous51411391
103609176336091764AG12GENIChomozygous51411426
103609191136091912CG13GENICheterozygous51411428
103609199536091996AAGCT11GENIChomozygous51411430
103609200036092001C-11GENIChomozygous51411432
103609214236092143CT15GENICheterozygous51411434
103609247436092475TC16GENIChomozygous51411436
103609259636092597TA24GENIChomozygous51411438
103609277036092771CG20GENIChomozygous51411440
103609286336092864CT12GENIChomozygous51411442
103609292736092928AG14GENIChomozygous51411444
103609294136092942CT18GENIChomozygous51411446
103609307136093072AG16GENIChomozygous51411448
103609311236093113TC16GENIChomozygous51411450
103609376536093766TA22GENIChomozygous51411452
103609385036093851CG22GENIChomozygous51411454
103609401236094013GT19GENIChomozygous51411456
103609417836094187CATCTGCAC---------13GENIChomozygous51411458
103609176836091769TC13GENICheterozygous52039185
103609194736091948GA11GENICheterozygous52039187
103609237436092375TC9GENICheterozygous52039189