chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105501781055017811TG26GENICpossibly homozygous661268636
105502275355022754GGC14GENIChomozygous763838673
105502651655026517AG34GENIChomozygous661268637
105503269255032694TT--11GENICheterozygous763838674
105503269355032694T-11GENICpossibly homozygous763838675
105503666955036670CCTCTATCTA6GENIChomozygous763838677
105503704355037044TTTCTA7GENIChomozygous763838679
105503718655037188AC--1GENIChomozygous763838683
105503910655039114ACACACAC--------5GENIChomozygous763838685
105504050255040503GA10GENIChomozygous661268638
105504050355040504TC9GENIChomozygous661268639
105504050755040508TC11GENIChomozygous661268640
105504052255040523GA7GENIChomozygous661268641
105504611055046113CTT---17GENIChomozygous763838689
105504621355046214TC16GENIChomozygous661268642
105505394555053946AATGGGCTGGAGAGATGGCTCGGTGGTTAAGAGCCCCAACTGCTCTTCCATAGGTCCTTAGTTC11GENIChomozygous763838690
105505672055056736ACACACACACACACAC----------------7GENICpossibly homozygous763838692
105505748555057486GGTTTC4GENIChomozygous763838694
105505845855058459TC35GENIChomozygous661268643
105505936355059364TTTGTG9GENICheterozygous763838699
105506745155067452T-1GENIChomozygous763838700
105506841555068417CC--6GENICheterozygous763838702
105506841655068417C-6GENICheterozygous763838703
105507036355070364CA27GENIChomozygous661268644
105508075255080753AC29GENIChomozygous661268645
105508217255082174AC--2GENIChomozygous763838705
105509802755098028TA31GENIChomozygous661268646
105510062855100630TC--15GENIChomozygous763838706
105510398855104004GAGAGAGAGAGAGAGA----------------8GENIChomozygous763838710
105511057455110575CCTTGTTGTTG10GENIChomozygous763838713
105511591755115918CT23GENIChomozygous661268647
105511946055119468ACACACAC--------5GENIChomozygous763838716
105512680155126802AC28GENIChomozygous661268648
105512953755129538CCTT5GENIChomozygous763838719
105513384355133844GA28GENIChomozygous661268649
105514452555144526TTAAA5GENICheterozygous763838721