chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104590971545909716TC25GENICpossibly homozygous51443475
104591066645910667TC14GENIChomozygous51443476
104591071745910718GT8GENIChomozygous51443477
104591128245911285ATT---1GENIChomozygous51443478
104591128645911288TT--7GENICpossibly homozygous52373248
104591141145911412GGT10GENIChomozygous51443480
104591150845911509AACTCT3GENIChomozygous52373250
104591157145911572GGTGTGTGTA3GENICheterozygous52373252
104591157345911574GGTGTGTA3GENICheterozygous52600406
104591160245911604CA--3GENIChomozygous51443483
104591160745911608GT3GENIChomozygous51443484
104591161345911614GGT3GENIChomozygous51443485
104591166545911666CT5GENIChomozygous51443486
104591167745911678GA5GENIChomozygous51443487
104591168245911683CG5GENIChomozygous51443488
104591293845912939TC9GENIChomozygous51443489
104591355645913557AC17GENIChomozygous51443490
104591424645914247GT6GENIChomozygous51443491
104591439745914398TG9GENIChomozygous51443492
104591508345915085AA--10GENIChomozygous51443500
104591657645916577TC18GENIChomozygous51443502
104591747445917475GA16GENIChomozygous51443503
104591752245917523AG14GENIChomozygous51443504
104591792645917927TC17GENIChomozygous51443505
104591949245919493CT11GENIChomozygous51443506
104591958045919581AC8GENIChomozygous51443507
104592141345921421AAATAAAT--------7GENIChomozygous51443508
104592171345921716AAG---3GENIChomozygous52647988
104592229945922300GA6GENIChomozygous51443511
104592240145922402GA6GENIChomozygous51443512
104592403445924035AG9GENIChomozygous51443513
104592487645924877GA18GENIChomozygous51443514
104592677145926773TT--6GENIChomozygous51443515
104592740645927534CATACTTGAATTCTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCGT--------------------------------------------------------------------------------------------------------------------------------28GENIChomozygous52318014
104592773045927731TTCCAC9GENIChomozygous51443517
104592784345927844AG23GENIChomozygous51443518