chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
119015212690152127AG31GENIChomozygous50863164
119015248690152487CT20GENIChomozygous50863165
119015298890152989CCGTGTGT6GENICheterozygous50863166
119015298890152989CCGTGTGTGT6GENICheterozygous51192850
119015376990153770T-18GENIChomozygous50974627
119015416290154163T-34GENIChomozygous50863169
119015496090154961CT37GENIChomozygous51134860
119015531190155312AAT18GENIChomozygous50863172
119015558990155591GG--8GENICheterozygous50863174
119015715690157157AACTTC34GENIChomozygous50863178
119015743290157433AC40GENIChomozygous51134863
119015884890158849CT16GENIChomozygous50863182
119015893390158934TC21GENIChomozygous50863183
119016232290162323GGC24GENICheterozygous51197680
119016232490162325GGC12GENICheterozygous51192852
119016232590162326TG24GENICheterozygous51197681
119016232790162328TG12GENIChomozygous51192853
119016233090162331GGAGGA12GENICheterozygous51192854
119016233090162331GGGA12GENICheterozygous51197682
119016238090162381GC28GENIChomozygous50863191
119016238190162382TC27GENIChomozygous50863192
119016239490162395AG33GENIChomozygous50863193
119016239590162396TC33GENIChomozygous50863194
119016240990162410CG30GENIChomozygous50863195
119016249590162496TG34GENIChomozygous50863196
119016297890162979GGC28GENIChomozygous51134866
119016380390163804TG37GENIChomozygous50974639
119016404390164044AT41GENIChomozygous50863198
119016421290164213TC40GENIChomozygous50863199
119016433990164340TA43GENIChomozygous50863201
119016468590164686GA17GENIChomozygous50974640
119016487390164874AAT35GENIChomozygous50863202
119016492290164923CT29GENIChomozygous51134869
119016499590164996AAC26GENIChomozygous50974641
119016500290165003CT26GENIChomozygous50974642
119016504790165048GT37GENIChomozygous50863204
119016524690165247GA26GENIChomozygous50974643
119016558790165588TG25GENIChomozygous50863207
119016707790167078C-37GENIChomozygous51134875
119016733090167331GA27GENIChomozygous51134878
119016746790167468CT19GENIChomozygous51134881