chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31400351314003514GA21GENIChomozygous111452140
31400357814003579GC24GENIChomozygous111452141
31400393714003938GT24GENIChomozygous111452142
31400416914004170TC18GENIChomozygous111452143
31400418414004185GT17GENICpossibly homozygous111452144
31400451714004518TA15GENIChomozygous111452145
31400461614004617CT13GENIChomozygous111452146
31400656714006571ACAT11GENIChomozygous127851712
31400632414006324CA12GENICpossibly homozygous127851710
31400637914006379ATACACAC11GENIChomozygous127851711
31400822014008221GA21GENIChomozygous111452147
31400912014009121TG25GENIChomozygous111452148
31401006314010063CA24GENIChomozygous127851714
31401006414010064TAG24GENIChomozygous127851715
31401021014010211CA29GENIChomozygous111452149
31401038514010386T22GENIChomozygous127851716
31401078814010789TC13GENIChomozygous111452150
31401084814010849TC5GENIChomozygous111452151
31401572014015721TC3GENIChomozygous111879017
31401915414019154G18GENIChomozygous127851717
31401917314019173G19GENIChomozygous127851718
31401920114019201G20GENIChomozygous127851719
31401933814019338G16GENIChomozygous127851720
31401935514019355G17GENIChomozygous127851721
31401951414019515AC16GENIChomozygous111452152
31401952214019523GC19GENIChomozygous111452153
31401952314019524TC19GENIChomozygous111452154
31401958914019590C14GENIChomozygous127851722
31401977914019780AG24GENIChomozygous111452155
31402045314020454AG29GENIChomozygous111452156
31402108414021085GA23GENIChomozygous111452157
31402109814021099GA23GENIChomozygous111452158
31402147614021477TA18GENIChomozygous111452159
31402152514021526CT20GENIChomozygous111452160
31402178214021783CT24GENIChomozygous111452161
31402287414022892CGAGAAACTCAGCACACA16GENIChomozygous127851723