chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6136058386136058387TA14GENIChomozygous115228769
6136060752136060753TC25GENIChomozygous114994681
6136065446136065447TC15GENIChomozygous115082182
6136069200136069201AG21GENIChomozygous115082183
6136084212136084213GA3GENIChomozygous114994690
6136084230136084231CA6GENIChomozygous114994691
6136084277136084278AC10GENIChomozygous114994692
6136084376136084377CT11GENIChomozygous114994693
6136084444136084445GC10GENIChomozygous114994695
6136086338136086339AT31GENIChomozygous115082185
6136092690136092691GA3GENIChomozygous114994702
6136095774136095775CA17GENIChomozygous114994706
6136100437136100438AT11GENIChomozygous114994708
6136100695136100696AT5GENIChomozygous114994709
6136105031136105032CA16GENIChomozygous114994712
6136105039136105040CT14GENIChomozygous114994713
6136107976136107977AT20GENICpossibly homozygous114994715
6136108046136108047GA15GENIChomozygous114994716
6136108075136108076GA15GENIChomozygous114994717
6136109355136109356GA3GENIChomozygous114994718
6136112933136112934TG9GENICpossibly homozygous115166391
6136116815136116816TG31GENIChomozygous114994723
6136118448136118449AC27GENIChomozygous115082188
6136118550136118551CG22GENIChomozygous114994725
6136118704136118705CT30GENIChomozygous114994726
6136118739136118740CT28GENIChomozygous114994727
6136119110136119111TC27GENIChomozygous114994728
6136119262136119263CG21GENIChomozygous115082189
6136121753136121754GT16GENICheterozygous115228770
6136122487136122488AG29GENIChomozygous115082191
6136122708136122709TG31GENIChomozygous115082192
6136124720136124721TA33GENIChomozygous115082193
6136125833136125834CT18GENIChomozygous115082194
6136125836136125837TC17GENIChomozygous114994741
6136129483136129484AC33GENICpossibly homozygous114994744