chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1196494034196494035TC59GENIChomozygous135782250
1196494254196494254CTT42GENIChomozygous135453251
1196494530196494531A48GENIChomozygous135453252
1196494805196494807CC39GENICheterozygous135453253
1196495581196495582TC52GENIChomozygous135782251
1196495678196495679CA61GENICpossibly homozygous135782252
1196495788196495789TG63GENIChomozygous135782253
1196496014196496015CA36GENICpossibly homozygous135782254
1196496388196496389CT26GENIChomozygous135782255
1196496543196496544CT37GENIChomozygous135782256
1196496726196496727GA41GENIChomozygous135782257
1196497509196497510AG50GENIChomozygous135782258
1196497786196497787GC43GENIChomozygous135782259
1196498032196498033AG35GENIChomozygous135782260
1196498112196498113CG22GENIChomozygous135782261
1196498257196498258AG49GENIChomozygous135782262
1196499258196499259CT45GENIChomozygous135782263
1196499840196499841CT15GENIChomozygous135782264
1196500195196500198TGT33GENIChomozygous135453257
1196495204196495205T46GENIChomozygous135453254
1196496102196496104AC28GENIChomozygous135453255
1196500032196500040TCTTTTTC19GENIChomozygous135453256
1196500199196500216TGTATGTATGTATGTAT33GENIChomozygous135453258
1196500515196500516GA26GENIChomozygous135782265
1196500661196500662AC44GENIChomozygous135782266
1196500867196500868TC47GENIChomozygous135782267
1196502710196502711GA79GENIChomozygous135782268