chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129750385129750386CG27GENIChomozygous115888121
7129752189129752190AG33GENIChomozygous115888123
7129752583129752584CT38GENIChomozygous115888125
7129754653129754654CT22GENIChomozygous115888127
7129754696129754697AC25GENIChomozygous115888129
7129755094129755095AG22GENIChomozygous115888131
7129755095129755096TC22GENIChomozygous115888133
7129755102129755103AC20GENIChomozygous115888135
7129755363129755364TC32GENICheterozygous115888137
7129755494129755495CA21GENIChomozygous115888139
7129757385129757386TC26GENIChomozygous115888141
7129757806129757807CG25GENIChomozygous115888143
7129757814129757815GA24GENIChomozygous115888145
7129758133129758134GA29GENIChomozygous115888147
7129758245129758246GA42GENIChomozygous115888149
7129758663129758664AG32GENIChomozygous115888151
7129761231129761232AG29GENIChomozygous115888153
7129761644129761645GA38GENIChomozygous115888155
7129762377129762378AG37GENIChomozygous115888157
7129764826129764827CT31GENIChomozygous115888159
7129766476129766477TA22GENIChomozygous115888161
7129767983129767984AG28GENIChomozygous115888163
7129768161129768162CT23GENIChomozygous115888165
7129768752129768753GA28GENIChomozygous115888167
7129769202129769203CA58GENICheterozygous115888169
7129769295129769296AG30GENICpossibly homozygous115888173
7129769366129769367AC26GENIChomozygous115888175
7129769872129769873GC20GENIChomozygous115888177
7129770736129770737AG28GENICpossibly homozygous115888179
7129770742129770743CT30GENICpossibly homozygous115888181
7129770765129770766TC28GENIChomozygous115888183
7129771113129771114GA33GENIChomozygous115888185
7129773002129773003TC26GENIChomozygous115888187
7129775736129775737CT25GENIChomozygous115888189
7129776944129776945TC26GENIChomozygous115888191
7129777541129777542GA11GENIChomozygous115888193
7129777543129777544CT11GENIChomozygous115888195
7129780665129780666TC35GENICpossibly homozygous115888197
7129782981129782982GA32GENIChomozygous115888199
7129783491129783492CT37GENIChomozygous115888201