chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118045556680455567GA13GENIChomozygous50969399
118045560780455608GT13GENIChomozygous50969400
118045611080456111AG7GENIChomozygous50969401
118045635180456352GA7GENIChomozygous50969402
118045701280457013CCT3GENIChomozygous51593402
118045710280457103A-7GENIChomozygous51593404
118045712280457123CCAA7GENIChomozygous51593406
118045731480457315CT7GENIChomozygous51593408
118045732280457324CC--4GENIChomozygous51593410
118045799480457995CCG2GENIChomozygous51288667
118045872080458724AAAC----9GENIChomozygous50969410
118045996380459964AG5GENIChomozygous51593412
118046089680460897AG9GENIChomozygous51237800
118046238480462385TTAA9GENIChomozygous51523845
118046274080462741GA7GENIChomozygous51593414
118046283880462839GA6GENIChomozygous50969411
118046568780465688AG15GENIChomozygous51593416
118046712580467127CA--3GENICheterozygous51190816
118046843780468438CT5GENIChomozygous51593418
118046929380469294C-10GENIChomozygous51593420
118046953880469572GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGG----------------------------------7GENICheterozygous51593422
118046992380469928TTTTT-----10GENIChomozygous50992713
118047047280470473AACTACGAGTCT4GENIChomozygous51593424
118047149980471500TTA7GENICpossibly homozygous51243667
118047240480472405CT5GENIChomozygous51237806
118047414680474147GGTTT9GENIChomozygous51593426
118047495380474954TTACAC1GENIChomozygous50969426
118047607180476072CT5GENIChomozygous51022077