chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103607921836079219CT18GENIChomozygous51848958
103607934336079344AG16GENIChomozygous51411305
103607963036079631AG11GENIChomozygous51411307
103607969736079698AG16GENIChomozygous51411309
103608006636080067AG20GENIChomozygous51411313
103608011936080120GC18GENIChomozygous51411315
103608029036080291CG16GENIChomozygous51848962
103608057336080574AG19GENIChomozygous51848965
103608077936080780A-8GENIChomozygous51411319
103608095936080960TC8GENIChomozygous51411321
103608165536081656AAT10GENIChomozygous51848968
103608497336084974AC25GENIChomozygous51411339
103608500636085007TC21GENIChomozygous51411341
103608543336085434TC43GENICheterozygous51411347
103608545736085458GA51GENICheterozygous51411349
103608551736085518GA42GENICheterozygous51411351
103608602336086024GGCATA6GENICheterozygous51848974
103608610736086108AT17GENIChomozygous51411359
103608674436086745CT21GENIChomozygous51848976
103608850336088504CT20GENICheterozygous51848979
103608850336088504CCT12GENIChomozygous51848982
103608869536088696TC23GENIChomozygous51411391
103609176336091764AG27GENIChomozygous51411426
103609191136091912CG28GENIChomozygous51411428
103609199536091996AAGCT30GENIChomozygous51411430
103609200036092001C-30GENIChomozygous51411432
103609214236092143CT30GENIChomozygous51411434
103609247436092475TC23GENIChomozygous51411436
103609259636092597TA27GENICpossibly homozygous51411438
103609277036092771CG22GENIChomozygous51411440
103609286336092864CT17GENIChomozygous51411442
103609292736092928AG10GENIChomozygous51411444
103609311236093113TC19GENIChomozygous51411450
103609294136092942CT6GENIChomozygous51411446
103609307136093072AG20GENIChomozygous51411448
103609376536093766TA20GENIChomozygous51411452
103609385036093851CG19GENIChomozygous51411454
103609401236094013GT23GENIChomozygous51411456
103609417836094187CATCTGCAC---------14GENIChomozygous51411458