chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109215292109215293AG14GENICpossibly homozygous670982232
6109215591109215592GGT15GENIChomozygous768895577
6109215956109215957CT16GENICpossibly homozygous670982233
6109216387109216389GT--18GENICheterozygous768895578
6109217437109217438GA13GENICheterozygous670982234
6109218533109218534TC3GENICheterozygous670982235
6109219644109219645CG2GENICheterozygous670982236
6109220171109220172AG17GENICheterozygous670982237
6109220957109220958T-1GENIChomozygous768895580
6109220959109220971TATACATGTTAT------------2GENIChomozygous768895581
6109221479109221480AG16GENIChomozygous670982238
6109222374109222375TTTCCAGCCC1GENIChomozygous768895582
6109222377109222378TTTGTTTTATTTAATAACCCA1GENIChomozygous768895583
6109225632109225633TC20GENIChomozygous670982239
6109225969109225970GC9GENICheterozygous670982240
6109226303109226304G-11GENIChomozygous768895584
6109226595109226596GA17GENICheterozygous670982241
6109226868109226869CCT6GENICheterozygous768895586
6109227291109227292CCTGTTT1GENIChomozygous768895587
6109227301109227302CCTGTTTGTTTGTT1GENIChomozygous768895590
6109227384109227385TC21GENICpossibly homozygous670982242
6109227502109227503GA4GENIChomozygous670982243
6109227690109227691AT25GENICpossibly homozygous670982244
6109227989109227990AG12GENICpossibly homozygous670982245