chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5148635719148635720CT48GENIChomozygous114154192
5148637758148637759TA40GENIChomozygous114154194
5148637828148637829AG35GENIChomozygous114154195
5148638149148638150CT8GENICheterozygous114154197
5148638313148638314GA44GENIChomozygous114154198
5148638508148638509AG33GENIChomozygous114154199
5148638964148638965GA41GENIChomozygous114154200
5148645596148645597GC39GENIChomozygous114154201
5148646075148646076CA36GENIChomozygous114154202
5148647457148647458GA28GENIChomozygous114154203
5148647883148647884GT17GENIChomozygous114049847
5148647910148647911CT11GENIChomozygous114049849
5148647917148647918TG9GENIChomozygous114049851
5148647921148647922CG9GENIChomozygous114049853
5148651456148651457TG53GENICheterozygous114049855
5148652711148652712TC30GENIChomozygous114154204
5148653484148653485GA29GENIChomozygous114154205
5148653882148653883TC30GENIChomozygous114049857
5148656461148656462GC43GENIChomozygous114154207
5148661322148661323CT30GENIChomozygous114154208
5148661856148661857GA31GENIChomozygous114154209
5148662007148662008AG43GENICpossibly homozygous114154210
5148662973148662974GC32GENIChomozygous114154211
5148663545148663546CT38GENIChomozygous114154212
5148663601148663602GC39GENIChomozygous114154213
5148663830148663831AG34GENIChomozygous114154214
5148663996148663997CA30GENIChomozygous114154215
5148664381148664382AG49GENIChomozygous114154216
5148664727148664728GT21GENIChomozygous114049859
5148664729148664730GC21GENIChomozygous114049861
5148664731148664732GC21GENIChomozygous114049863
5148664732148664733GA21GENIChomozygous114049865
5148664737148664738GC22GENIChomozygous114049867
5148664792148664793AT28GENIChomozygous114154217
5148669253148669254TC56GENICheterozygous114154218
5148669264148669265GC54GENICheterozygous114154219
5148669266148669267GA54GENICheterozygous114154220
5148669272148669273CT52GENICheterozygous114154221
5148669274148669275CT51GENICheterozygous114154222