chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17943130479431305TA19GENIChomozygous60746021
17943133979431340AG17GENIChomozygous61444050
17943225079432251AG27GENIChomozygous61444051
17943326279433263CT16GENIChomozygous61444052
17943518179435182AAAAAT6GENIChomozygous61444053
17944113279441133AAG14GENIChomozygous60746022
17944289679442897T-19GENICpossibly homozygous61444054
17944340879443409CG16GENICheterozygous61444055
17944342279443423GC21GENICheterozygous61444056
17944345279443453GC22GENICheterozygous61444057
17944346379443465AC--18GENICheterozygous61444058
17944351579443519AGAC----11GENICpossibly homozygous61296907
17944352779443528AT16GENICheterozygous61444059
17944353179443532AT16GENICheterozygous61444060
17944359079443591GGGA9GENIChomozygous61444061
17944384879443849CT23GENIChomozygous61444062
17944415079444151TTAC4GENICheterozygous61444063
17944443179444432CT18GENIChomozygous61444064
17944456079444561AG22GENIChomozygous61444065
17944486879444869TC25GENIChomozygous61444066
17944491079444911C-21GENIChomozygous60746023
17944494579444946AC18GENIChomozygous61444067
17944631279446313AG19GENIChomozygous61444068
17944809679448097CT25GENICpossibly homozygous61444069