chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
911620191162020GT6GENICheterozygous877768110
912419531241954CG12GENIChomozygous877768111
912420671242068GT7GENIChomozygous877768112
912833331283334CA8GENIChomozygous877768113
912833561283357GC7GENIChomozygous877768114
912920261292027AT3GENICheterozygous877768115
913929041392905GA5GENICheterozygous877768116
914028001402801GA12GENICheterozygous877683772
914033641403365AT4GENIChomozygous877683763
914034081403409CT12GENICheterozygous877773543
914035361403537GA3GENICheterozygous877772705
914044311404432GT11GENIChomozygous877683762
914044651404466AG11GENIChomozygous877683761
914047361404737CT9GENICheterozygous877773546
914055481405549AC10GENICheterozygous877772710
914082081408209CG22GENICheterozygous877768167
914082381408239CA13GENICheterozygous877768166
914083351408336GT9GENICheterozygous877683745
914094241409425TA5GENICheterozygous877772685
914294901429491GT12GENICheterozygous877772708
914295001429501TG12GENICheterozygous877772707
914303481430349AT4GENIChomozygous877772714
914339701433971GT7GENICheterozygous877772706
914393871439388CG7GENICheterozygous877773619
914397221439723GT6GENIChomozygous877683693
914597731459774TC3GENICheterozygous877768117
914623911462392CT6GENICheterozygous877768118
915392891539290TC15GENIChomozygous877768119
915702591570260CA3GENICheterozygous877768120
915883561588357CT6GENIChomozygous877768121
915938631593864CA12GENIChomozygous877768122
915938901593891CT5GENIChomozygous877768123
916980071698008GC3GENICheterozygous877774239
917033291703330GT6GENIChomozygous877768124
917065871706588CA11GENIChomozygous877768125