chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108612621686126217GA14GENIChomozygous138842089
108612713186127132GA23GENIChomozygous138842090
108612895286128953CT20GENIChomozygous143463596
108612907886129081TTG28GENIChomozygous138696919
108612968786129688TA25GENIChomozygous138842091
108612992986129930GA13GENIChomozygous138842092
108613173686131737TC32GENIChomozygous138842093
108613285686132856T18GENIChomozygous138696921
108613476186134762AT9GENIChomozygous138842095
108613508686135087GA21GENIChomozygous138842096
108613632986136330AC16GENIChomozygous138842097
108613764886137648G31GENIChomozygous138696922
108613893686138937CT21GENIChomozygous138842104
108613655786136558AG24GENIChomozygous138842098
108613720986137210TC17GENIChomozygous138842099
108613749886137499CT21GENIChomozygous138842100
108613779886137799AG22GENIChomozygous138842101
108613830686138307CT19GENIChomozygous138842103
108613894886138949AG21GENIChomozygous138842105
108613933686139340TTTG19GENIChomozygous138696923
108614085586140856AG10GENIChomozygous138842106
108614147186141472TA13GENIChomozygous143463597
108614236186142361CC12GENIChomozygous138696924
108614241586142416CA15GENIChomozygous143463598
108614781986147820TC20GENIChomozygous138842113
108613825386138254C20GENICheterozygous403293715
108613825386138254CT20GENIChomozygous403293716
108614844586148446TA9GENICheterozygous154661524
108614844586148446TG9GENICheterozygous403293717
108614844586148446T9GENICheterozygous403293718