chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124248766542487666AC18GENIChomozygous50209167
124248770642487707CT20GENIChomozygous50209168
124248772942487730TC25GENIChomozygous50209169
124248811342488114AATTTTT10GENICheterozygous50544352
124248841242488421TTTTTTTAA---------19GENICpossibly homozygous50209173
124248897242488973GA55GENIChomozygous50209174
124249034742490348TA50GENIChomozygous50209175
124249053842490539AG42GENIChomozygous50209176
124249060142490602GA8GENIChomozygous50544353
124249060242490603CCACACACACA8GENIChomozygous50209179
124249065742490658CT30GENIChomozygous50209180
124249139342491394CT24GENIChomozygous50209181