chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5137268621137268622TC23INTERGENIChomozygous55744611
5137268982137268983GC15INTERGENIChomozygous55744612
5137269197137269198TC29INTERGENIChomozygous55901228
5137270244137270245GA60INTERGENIChomozygous55901229
5137270305137270306CT55INTERGENIChomozygous55901230
5137271318137271319AG30INTERGENIChomozygous55744615
5137271391137271392GA22INTERGENIChomozygous55901231
5137271547137271548TC28INTERGENIChomozygous55744616
5137271957137271958CT30INTERGENIChomozygous55744618
5137272263137272264TG26INTERGENIChomozygous55901232
5137275480137275510CCTCCGCTTCCTCCTCCAGCCAGGGGGTCT------------------------------6INTERGENIChomozygous56456816
5137275921137275925TGAG----39INTERGENIChomozygous55744621
5137277292137277316CACCATCACCATCACCATCACCAT------------------------22INTERGENIChomozygous56456817
5137277788137277789AAGGGG3INTERGENICheterozygous55901235
5137277788137277789AAGGG3INTERGENICheterozygous56456818
5137278206137278207CT32INTERGENIChomozygous55901236
5137278914137278915GA27INTERGENIChomozygous55901237
5137279260137279261AG28INTERGENIChomozygous55744623
5137279316137279317AAC29INTERGENIChomozygous55901238
5137279317137279318TC29INTERGENIChomozygous56456819
5137280035137280036GA34INTERGENIChomozygous55901239
5137280754137280755TC32INTERGENIChomozygous55901240
5137281316137281317CT29INTERGENICpossibly homozygous55901241
5137281701137281702TC35INTERGENIChomozygous55901242
5137281847137281848AG36INTERGENIChomozygous55901243