chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161304497161304498TC41GENIChomozygous111797085
3161305311161305312CT92GENIChomozygous111797087
3161305894161305895GA20GENIChomozygous111797089
3161307800161307801AG12GENICheterozygous119652597
3161308939161308940GA56GENIChomozygous111797093
3161310321161310322TC54GENIChomozygous111797097
3161311081161311082TC57GENIChomozygous111797099
3161313408161313409AG49GENICpossibly homozygous111797103
3161313445161313446GA39GENIChomozygous111797104
3161315032161315033TA7GENIChomozygous112045579
3161317592161317593TC55GENIChomozygous111797108
3161319012161319013TA21GENIChomozygous111797112
3161320379161320380TA6GENIChomozygous111797114
3161320441161320442AG11GENIChomozygous111797116
3161320894161320895AT4GENIChomozygous120020232
3161321135161321136TC43GENIChomozygous111797124
3161321825161321826CT56GENIChomozygous119652600
3161321826161321827TG58GENIChomozygous119652601
3161322054161322055CT67GENIChomozygous111797126
3161322099161322100AG58GENIChomozygous111797128