chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104591066645910667TC24GENIChomozygous51443476
104591150845911509AACTCT2GENIChomozygous52373250
104591160245911604CA--5GENICheterozygous51443483
104591161345911614GGT9GENIChomozygous51443485
104591166545911666CT10GENIChomozygous51443486
104591167745911678GA10GENIChomozygous51443487
104591168245911683CG10GENIChomozygous51443488
104591246145912462GT18GENIChomozygous52193637
104591293845912939TC16GENIChomozygous51443489
104591508345915085AA--15GENICheterozygous51443500
104591508445915085A-15GENICpossibly homozygous51443501
104591657645916577TC26GENIChomozygous51443502
104591792645917927TC35GENIChomozygous51443505
104591958045919581AC23GENIChomozygous51443507
104591993845919939TA21GENIChomozygous52193643
104592141745921421AAAT----13GENIChomozygous51636534
104592170245921703A-19GENICpossibly homozygous51443509
104592275745922758GA10GENIChomozygous52193645
104592403445924035AG15GENICpossibly homozygous51443513
104592653045926531CT37GENIChomozygous52193647
104592677045926771AAT16GENICheterozygous52496878
104592677145926773TT--16GENICheterozygous51443515
104592677245926773T-16GENICheterozygous51443516
104592740645927534CATACTTGAATTCTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCGT--------------------------------------------------------------------------------------------------------------------------------30GENIChomozygous52318014
104592784345927844AG30GENIChomozygous51443518
104591449145914492AAGGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGCAATCCTGTCTCCCACCCTGAAATCC4GENIChomozygous52459279