chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74201468542014686TG31GENIChomozygous54194437
74201468642014687AT31GENIChomozygous53891807
74201532542015326GA35GENIChomozygous53891808
74201608342016084AG33GENIChomozygous53891809
74201674942016750GGACAC5GENICheterozygous53891810
74201674942016750GGAC5GENICheterozygous55275067
74201697042016971T-21GENIChomozygous53891811
74201698042016981AG21GENIChomozygous53891812
74201725342017254AG27GENIChomozygous53891813
74202070942020719AAGAGACAGA----------19GENIChomozygous53891815
74202133242021333TG27GENIChomozygous53891817
74202262542022626TC38GENIChomozygous53891818
74202484742024848CT10GENIChomozygous53891819
74202779142027792TC33GENIChomozygous53891820
74202862142028622TC19GENIChomozygous53891821
74202881442028815CCT21GENIChomozygous53891822
74202891742028918AC1GENIChomozygous54194438
74202891942028920TG1GENIChomozygous54194439
74202892342028927AGGA----1GENIChomozygous53891824
74202900042029001C-3GENIChomozygous53891835
74202900842029009G-3GENIChomozygous53891836
74202901442029015AAT4GENIChomozygous53891837
74202902042029021G-6GENIChomozygous53891838
74202931242029313TC24GENIChomozygous53891839
74202946542029466TC19GENIChomozygous53891840
74202969342029694CT35GENIChomozygous53891841
74203043642030437GGA26GENICpossibly homozygous53891842
74203070142030702AT20GENIChomozygous53891843
74203112642031127AG14GENIChomozygous53891844
74203183442031835AG25GENIChomozygous53891845
74201886942018870CCCT15GENIChomozygous56003185