chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147537153147537154GA34GENIChomozygous114046166
5147537211147537212GT30GENIChomozygous114046167
5147537269147537270GT35GENICpossibly homozygous114046169
5147537684147537685CT63GENIChomozygous114046171
5147538543147538544GA46GENIChomozygous114046173
5147540579147540580AG31GENIChomozygous114046175
5147540591147540592AG34GENIChomozygous114046177
5147541272147541273GA33GENIChomozygous114046179
5147541520147541521TG64GENIChomozygous114046181
5147541547147541548CG59GENIChomozygous114046183
5147541931147541932AG48GENICheterozygous114046185
5147541939147541940AG44GENICpossibly homozygous114046187
5147542451147542452AG3GENIChomozygous114046189
5147542484147542485CG12GENIChomozygous114046191
5147543257147543258TC36GENICheterozygous114046193
5147543872147543873CT51GENIChomozygous114046195
5147544730147544731AG11GENIChomozygous114046197
5147544904147544905CT49GENIChomozygous114046199
5147546105147546106TC37GENIChomozygous114046201