chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104068740640687407T-6GENICheterozygous51426289
104069820940698210CT11GENICheterozygous52187134
104070152240701523A-7GENICpossibly homozygous51426315
104071320640713207TC9GENICheterozygous51426385
104072054840720549CA8GENICheterozygous52187258
104072091740720918TC14GENIChomozygous51426416
104074655840746559CCA12GENIChomozygous51426517
104075664140756642GGGCAT7GENIChomozygous52316629
104077080440770822GGTGTGTGTGTGTGCAGG------------------4GENICheterozygous52600081
104077113740771138CT5GENIChomozygous51426607
104077114340771144AG4GENIChomozygous51426608
104077115140771152CG1GENIChomozygous51426609
104077116340771164CG1GENIChomozygous51426610
104077117640771177CA2GENIChomozygous52316633
104077117840771179AG3GENIChomozygous52316634
104077119240771193GA13GENICheterozygous52316636
104077119340771194AG13GENICheterozygous52316638