chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397277149727715TA33GENIChomozygous112065341
397306369730637GA10GENIChomozygous112065353
397307899730790AG23GENIChomozygous112065355
397314939731494TC18GENIChomozygous112330363
397318429731843TC31GENIChomozygous112065357
397318439731844CG34GENIChomozygous119912614
397329389732939GA30GENIChomozygous112065363
397325309732531AC16GENIChomozygous112065361
397339819733982CA26GENIChomozygous112065365
397339829733983CT26GENIChomozygous112065367
397341869734187CT33GENIChomozygous112065369
397342189734219CT26GENIChomozygous112065371
397343089734309TC18GENIChomozygous112065373
397345049734505AG19GENIChomozygous112065375
397346279734628AG21GENIChomozygous112065377
397348749734875GA29GENIChomozygous112065379
397350719735072AG29GENIChomozygous112065381
397351279735128CT30GENIChomozygous112330365
397355439735544AG15GENICpossibly homozygous112065383
397361879736188TC31GENIChomozygous112065387
397372569737257CT30GENIChomozygous112065389
397376179737618AG25GENIChomozygous112330367
397377029737703CT25GENIChomozygous112330369
397380419738042GC23GENIChomozygous112065391
397381169738117TC22GENIChomozygous112065393
397381499738150AG19GENIChomozygous112065395