chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136733687136733688TC31GENIChomozygous114020631
5136734219136734220TC24GENIChomozygous114020633
5136734846136734847GA25GENIChomozygous114020635
5136735308136735309CA28GENIChomozygous114020637
5136735435136735436GA29GENIChomozygous114020639
5136736239136736240GA23GENIChomozygous114020641
5136738047136738048AG35GENIChomozygous114020642
5136739230136739231AC21GENIChomozygous114020644
5136739411136739412CT18GENIChomozygous114020646
5136740341136740342TC20GENIChomozygous114020648
5136740572136740573AG17GENIChomozygous114020650
5136740810136740811CT21GENIChomozygous114020652
5136740912136740913GA27GENIChomozygous114020654
5136742263136742264CA25GENICheterozygous114020656
5136742271136742272CA24GENIChomozygous114020658
5136742283136742284AC20GENICpossibly homozygous114020660
5136744959136744960GA28GENIChomozygous114020662
5136746896136746897GA14GENIChomozygous114020664
5136747566136747567GA33GENIChomozygous114020666
5136747767136747768AG29GENIChomozygous114020668
5136748497136748498CA35GENIChomozygous114020670