chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99250610192506102AG33GENIChomozygous117600946
99250768692507686TG27GENIChomozygous128732072
99250792792507927TG6GENICheterozygous132412856
99251094492510945CA17GENIChomozygous120385827
99251096392510963T15GENIChomozygous130380140
99251096592510966CA12GENIChomozygous130388531
99251097592510976GT13GENIChomozygous130388532
99251097792510985GTGAGGAG13GENIChomozygous130380141
99251098792510987TATGT11GENIChomozygous130380142
99251099592510996G17GENIChomozygous130380143
99251099692510997CT17GENIChomozygous130388533
99251099992511000CA17GENIChomozygous130388534
99251100292511003CA18GENIChomozygous130388535
99251100592511006GA22GENIChomozygous130388536
99251100992511010CA24GENIChomozygous130388537
99251101292511013GC24GENIChomozygous130388538
99251102892511029CA29GENIChomozygous130388539
99251103092511031CA29GENIChomozygous130388540
99251103492511035C30GENIChomozygous130380144
99251104392511044TG34GENIChomozygous130388541
99251104592511046GC35GENIChomozygous130388542
99251104892511048T36GENIChomozygous130380145
99251105392511053CT37GENIChomozygous130380146
99252515192525151A22GENIChomozygous128732079
99252515592525155AG22GENIChomozygous128732080
99252515992525159C22GENIChomozygous128732081
99252531192525311A28GENIChomozygous128732082
99252753092527539CCCCCCCCC38GENIChomozygous128732084