chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
397277149727715TA36GENIChomozygous112065341
397306369730637GA17GENIChomozygous112065353
397307899730790AG23GENIChomozygous112065355
397314939731494TC18GENIChomozygous112330363
397325309732531AC17GENIChomozygous112065361
397329389732939GA31GENIChomozygous112065363
397339819733982CA25GENIChomozygous112065365
397339829733983CT25GENIChomozygous112065367
397341869734187CT33GENIChomozygous112065369
397342189734219CT26GENIChomozygous112065371
397343089734309TC18GENIChomozygous112065373
397345049734505AG20GENIChomozygous112065375
397346279734628AG25GENIChomozygous112065377
397348749734875GA30GENIChomozygous112065379
397350719735072AG30GENIChomozygous112065381
397351279735128CT30GENIChomozygous112330365
397355439735544AG24GENICpossibly homozygous112065383
397357099735710TA24GENIChomozygous112065385
397361879736188TC32GENIChomozygous112065387
397372569737257CT30GENIChomozygous112065389
397376179737618AG26GENIChomozygous112330367
397377029737703CT25GENIChomozygous112330369
397380419738042GC23GENIChomozygous112065391
397381169738117TC22GENIChomozygous112065393
397381499738150AG19GENIChomozygous112065395