chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119015212690152127AG33GENIChomozygous50863164
119015248690152487CT21GENIChomozygous50863165
119015298890152989CCGTGT5GENICheterozygous51192849
119015298890152989CCGTGTGTGT5GENICheterozygous51192850
119015303990153041TA--14GENICheterozygous51192851
119015376990153770T-28GENIChomozygous50974627
119015416290154163T-35GENIChomozygous50863169
119015496090154961CT29GENIChomozygous51134860
119015531190155312AAT22GENIChomozygous50863172
119015715690157157AACTTC30GENIChomozygous50863178
119015743290157433AC36GENIChomozygous51134863
119015884890158849CT28GENIChomozygous50863182
119015893390158934TC37GENIChomozygous50863183
119016232490162325GGC6GENICheterozygous51192852
119016232790162328TG5GENICheterozygous51192853
119016233090162331GGAGGA5GENICheterozygous51192854
119016238090162381GC22GENIChomozygous50863191
119016238190162382TC23GENIChomozygous50863192
119016239490162395AG26GENIChomozygous50863193
119016239590162396TC26GENIChomozygous50863194
119016240990162410CG31GENIChomozygous50863195
119016249590162496TG29GENIChomozygous50863196
119016297890162979GGC18GENIChomozygous51134866
119016380390163804TG35GENIChomozygous50974639
119016404390164044AT34GENIChomozygous50863198
119016421290164213TC29GENIChomozygous50863199
119016433990164340TA43GENIChomozygous50863201
119016468590164686GA33GENIChomozygous50974640
119016487390164874AAT48GENIChomozygous50863202
119016492290164923CT35GENIChomozygous51134869
119016499590164996AAC30GENIChomozygous50974641
119016500290165003CT33GENIChomozygous50974642
119016504790165048GT32GENIChomozygous50863204
119016524690165247GA36GENIChomozygous50974643
119016558790165588TG21GENIChomozygous50863207
119016707790167078C-51GENIChomozygous51134875
119016733090167331GA37GENIChomozygous51134878
119016746790167468CT30GENIChomozygous51134881