chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147019424970194250AG21GENIChomozygous49124309
147019451170194512GA30GENIChomozygous49124311
147019476570194766AG21GENIChomozygous49124313
147019484970194851CC--16GENIChomozygous49124315
147019504570195046GA31GENIChomozygous49124317
147019513470195135GGA35GENIChomozygous49124318
147019567470195675GGA14GENIChomozygous49124320
147019638970196390AG11GENIChomozygous49124322
147019641170196412AG14GENIChomozygous49124324
147019683870196839GGT31GENIChomozygous48786163
147019717670197177C-25GENIChomozygous49124326
147019724170197242AAC18GENIChomozygous49124327
147019744470197445CT24GENIChomozygous49124329
147019802070198021AACT20GENIChomozygous49124331
147019813570198136AG30GENIChomozygous49124333
147019820270198203TG25GENIChomozygous49124335
147019832670198327CT34GENIChomozygous49124337
147019836570198366AC29GENIChomozygous49124339
147019841570198416CT19GENIChomozygous49124341
147019858970198590GA25GENIChomozygous49124343
147019872970198730CA16GENIChomozygous49124345
147019977370199774GGC20GENIChomozygous49124347
147020004770200051TCTG----3GENIChomozygous49124349
147020004770200048TTC3GENIChomozygous49124351
147020006870200069AG6GENIChomozygous49124353
147020026970200270CG18GENIChomozygous49124355
147020065470200655AG23GENIChomozygous49124357
147020083170200832GT30GENIChomozygous49124359
147020123370201234TG33GENICheterozygous49124361
147020141670201417GA32GENIChomozygous49124363
147020173370201734CA29GENIChomozygous49124365
147020175870201759CT23GENIChomozygous49124367
147020184070201841GA20GENIChomozygous49124369
147020216970202170GA25GENICheterozygous49124371
147020221370202214CG23GENICpossibly homozygous49124373
147020241170202412CT18GENIChomozygous49124375
147020278270202784GT--23GENIChomozygous49124377
147020338070203381T-29GENIChomozygous49124379
147020340270203403AT27GENIChomozygous49124380