chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116821549116821562TTTTTTTTTTTTT-------------4GENICheterozygous747611809
7116823142116823143TC33GENIChomozygous634722534
7116823343116823344T-22GENICpossibly homozygous747611810
7116823521116823522TC34GENIChomozygous634722535
7116824211116824212TC19GENIChomozygous634722536
7116825093116825094GA50GENIChomozygous634722537
7116825103116825104GA47GENIChomozygous634722538
7116825628116825629AT39GENIChomozygous634722539
7116825974116825975TTA23GENICheterozygous747611811
7116826213116826214CCA4GENICheterozygous747611812
7116826543116826544AG29GENIChomozygous634722540
7116826982116826983GA35GENIChomozygous634722541
7116828351116828352GT24GENIChomozygous634722542
7116829856116829857GT41GENIChomozygous634722543
7116832075116832076CCCTG29GENICpossibly homozygous747611813
7116832310116832311TG42GENICpossibly homozygous634722544
7116832608116832611AAA---15GENIChomozygous747611814
7116833888116833889TC52GENIChomozygous634722545
7116834093116834094AG54GENIChomozygous634722546
7116834099116834100TA57GENIChomozygous634722547
7116834100116834101CA56GENIChomozygous634722548
7116834256116834257A-33GENIChomozygous747611816
7116834291116834292CA27GENIChomozygous634722549
7116834292116834293TG26GENIChomozygous634722550
7116834416116834417AAACT23GENIChomozygous747611817