chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151319202151319203GA19GENIChomozygous137652182
5151322316151322317CT12GENIChomozygous137652183
5151324687151324701CACCCAGCCTCCAG19GENIChomozygous137349337
5151326328151326329GA20GENIChomozygous137652184
5151327095151327096G6GENICheterozygous403162989
5151327095151327096GC6GENICheterozygous403162990
5151327097151327098G6GENICheterozygous403162991
5151327097151327098GC6GENICheterozygous403162992
5151327099151327100GC6GENICheterozygous137652185
5151327099151327100G6GENICheterozygous403162993
5151327101151327102GC6GENICheterozygous137652186
5151327101151327102G6GENICheterozygous403162994
5151327103151327104GC8GENICheterozygous141766598
5151327484151327484C19GENIChomozygous137349338
5151328174151328175CT25GENIChomozygous137652187
5151329094151329101GACTTTG24GENIChomozygous137349339
5151329791151329792CT22GENIChomozygous137652188
5151329866151329867AG19GENIChomozygous137652189