chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3117793837117793837A29GENIChomozygous136586073
3117793838117793839GC30GENIChomozygous154134816
3117794219117794219C30GENICpossibly homozygous136586074
3117794320117794321TG25GENIChomozygous154134817
3117794857117794858GA42GENIChomozygous136799206
3117795860117795861GT39GENIChomozygous136799207
3117795939117795940CT33GENIChomozygous136799208
3117795995117795996AG43GENIChomozygous136799209
3117795999117796000GT44GENIChomozygous136799210
3117796566117796567AG49GENIChomozygous136799211
3117797361117797362TG33GENIChomozygous136799213
3117797854117797855GA62GENIChomozygous136799214
3117797888117797889TC64GENIChomozygous136799215
3117798158117798159AG34GENIChomozygous136799217
3117799749117799749A55GENIChomozygous136586076
3117799806117799807CT58GENIChomozygous143922383
3117794571117794572CA32GENIChomozygous143922380
3117795998117795999AT42GENIChomozygous143922381
3117798352117798353GA70GENICpossibly homozygous143922382
3117800397117800398TC49GENIChomozygous136799219
3117800567117800568AG57GENIChomozygous143922384
3117800686117800687AG51GENIChomozygous143922385
3117801134117801135CT40GENIChomozygous143922386
3117801175117801176GT35GENIChomozygous143922387
3117801234117801235GA37GENIChomozygous143922388
3117801462117801463AG19GENIChomozygous143922389
3117801939117801940AG64GENIChomozygous143922390
3117802218117802219GA35GENIChomozygous143922391
3117802493117802494TC55GENIChomozygous136799220
3117802793117802794TC43GENIChomozygous136799221
3117803568117803569AT36GENICheterozygous154134818
3117803888117803889CT55GENIChomozygous143922392
3117803567117803569TA36GENIChomozygous143863230
3117803568117803569A36GENIChomozygous403075669