chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123516888123516889AG11GENIChomozygous54090238
7123516890123516891AAG11GENIChomozygous54090239
7123520006123520007CT19GENIChomozygous54236443
7123520124123520125GA16GENIChomozygous54236445
7123520136123520137GA16GENIChomozygous54236447
7123520191123520192AG11GENIChomozygous54236449
7123520604123520605AG26GENIChomozygous54236451
7123521343123521344GA7GENIChomozygous54236453
7123521573123521574GC9GENIChomozygous54090251
7123522069123522070CT7GENIChomozygous54236455
7123522481123522482CT8GENIChomozygous54090256
7123522737123522738AC6GENIChomozygous54236461
7123522747123522748C-5GENIChomozygous54921462
7123522750123522752AC--6GENIChomozygous54236465
7123523179123523180GA13GENIChomozygous54236471
7123523421123523422CT14GENIChomozygous54236473
7123523513123523514TG26GENIChomozygous54090260
7123524797123524798GT17GENIChomozygous54236475
7123524801123524802CT16GENIChomozygous54090263
7123524844123524845AG11GENIChomozygous54236477
7123525305123525306CT14GENIChomozygous54236483
7123526279123526280AG12GENIChomozygous54236485
7123526699123526711TGATGATGATGG------------6GENIChomozygous55097233
7123526836123526837AT10GENIChomozygous54236491
7123527365123527366CT9GENIChomozygous54236493
7123528914123528915GGC9GENICheterozygous54236497
7123529263123529271TGTGTGTG--------13GENIChomozygous54236503
7123529754123529755AG16GENIChomozygous54236505
7123531193123531194TC12GENIChomozygous54236509