chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110220848110220849AG4GENIChomozygous138413351
8110222122110222122GAG16GENIChomozygous142030615
8110222409110222410TC21GENIChomozygous138413353
8110222634110222635CT15GENIChomozygous138413355
8110223374110223374CT5GENIChomozygous142030616
8110223376110223376CT5GENIChomozygous142030617
8110223379110223379TTCT5GENIChomozygous142030618
8110223900110223901AG20GENIChomozygous138413356
8110225490110225491AG28GENIChomozygous138413359
8110226367110226368CT21GENIChomozygous138413360
8110227163110227164AC15GENIChomozygous138413361
8110227457110227458AG26GENIChomozygous138413362
8110227473110227474CT25GENIChomozygous142100503
8110222858110222859GA30GENIChomozygous142100499
8110222905110222906CA21GENIChomozygous142100500
8110225534110225535GA26GENIChomozygous142100501
8110225561110225562GA26GENIChomozygous142100502
8110225417110225442ATTCTGGGCAAGACAAAAGCCCAGG27GENIChomozygous142030619
8110223387110223388TC5GENIChomozygous403727747
8110227821110227822T24GENIChomozygous142030620
8110228465110228466GA28GENIChomozygous142100504
8110229101110229102AG17GENIChomozygous138413364
8110229343110229344AG17GENIChomozygous138413365
8110229447110229449AT9GENIChomozygous142030621
8110229448110229449TA9GENICheterozygous154541840
8110229448110229449T9GENIChomozygous403248979
8110229597110229597TAGC13GENIChomozygous142030622
8110229839110229840TC21GENIChomozygous142100505
8110230216110230217TC25GENIChomozygous138413366
8110230481110230482AG24GENIChomozygous138413367
8110232259110232259CACACCTGCAGCCATGCACACCTGTAACCATG21GENIChomozygous142030623
8110233211110233212CT16GENIChomozygous142100506