chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812471263812472GA19GENIChomozygous971745299
1263813164263813165CA11GENIChomozygous971745300
1263813314263813315GA20GENIChomozygous971745301
1263813492263813493TA33GENIChomozygous971745302
1263814051263814052CT23GENIChomozygous971745303
1263815349263815350GA12GENIChomozygous971745304
1263815744263815745AG10GENIChomozygous971745305
1263817743263817744AG18GENIChomozygous971745306
1263820813263820814AG13GENIChomozygous971745307
1263820861263820862CT15GENIChomozygous971745308
1263821401263821402GA9GENIChomozygous971745309
1263823231263823232GA12GENIChomozygous971745310
1263823243263823244CT14GENIChomozygous971745311
1263823512263823513AG13GENIChomozygous971745312
1263825765263825766GT14GENIChomozygous971745313
1263827331263827332GA7GENIChomozygous971745314
1263828502263828503CA11GENIChomozygous971745315
1263829149263829150AT9GENICheterozygous971745316
1263831722263831723CT9GENIChomozygous971745317
1263832115263832116TC13GENIChomozygous971745318
1263832813263832814AG12GENIChomozygous971745319
1263835278263835279CT14GENIChomozygous971745320
1263835926263835927GA12GENIChomozygous971745321
1263837493263837494GA22GENIChomozygous971745322
1263840846263840847CT15GENIChomozygous971745323
1263842282263842283GT16GENIChomozygous971745324
1263843300263843301AT9GENIChomozygous971745325
1263844963263844964AG18GENIChomozygous971745326