chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6107738339107738340GA17GENIChomozygous71411835
6107742019107742020GA18GENIChomozygous71411839
6107743455107743456AG17GENIChomozygous71411841
6107743553107743554GT16GENIChomozygous71044094
6107746804107746805CG10GENIChomozygous71044097
6107747005107747006CT18GENIChomozygous71411843
6107747021107747022GA12GENIChomozygous71411845
6107747827107747828GT4GENIChomozygous71411847
6107748143107748144GA23GENIChomozygous71411849
6107748370107748371AG15GENIChomozygous71044100
6107752978107752979TA11GENIChomozygous72163591
6107741061107741062CT13GENIChomozygous72389132
6107741921107741921A5GENIChomozygous72817974
6107748902107748903TC9GENIChomozygous70526574
6107748917107748918GT5GENIChomozygous70526578
6107748920107748921AC5GENIChomozygous70526582
6107748926107748927CA6GENIChomozygous70526586
6107752945107752946CG18GENIChomozygous70526590
6107748965107748966G18GENICheterozygous72163576
6107752843107752844G18GENICheterozygous72163579
6107748969107748970CT16GENIChomozygous72030490
6107749604107749605AC5GENIChomozygous72030493
6107749605107749606TC4GENIChomozygous72030496
6107752975107752976GA11GENIChomozygous72163585
6107752976107752977AT11GENIChomozygous72163588
6107753009107753009T12GENICheterozygous72817976
6107754298107754299CT20GENIChomozygous71411853
6107771647107771648CG16GENIChomozygous71411857
6107753795107753796AT8GENIChomozygous72254494
6107775309107775310AC16GENIChomozygous71277522