chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104618405746184058CA57GENIChomozygous116585212
104618457846184578T51GENICpossibly homozygous128814161
104618469746184698CT56GENIChomozygous116585214
104618500246185003CT66GENIChomozygous116585216
104618503546185036AG66GENIChomozygous116585218
104618538346185384AG40GENIChomozygous117410415
104618575046185751TC35GENIChomozygous116585220
104618598046185981CT32GENIChomozygous117129048
104618737746187377T32GENICheterozygous128814162
104618741246187413CA38GENIChomozygous116585222
104618848946188491CA42GENIChomozygous128814163
104618960846189609AG49GENIChomozygous123441210
104618961446189615AG52GENIChomozygous123441211
104618962046189621AG50GENIChomozygous123441212
104618962646189627AG51GENIChomozygous116585224
104618963146189633TA50GENIChomozygous128814164
104618971346189721TATATGTG45GENIChomozygous128814165
104619051546190516TC82GENIChomozygous116585226
104619241646192417TG69GENIChomozygous116585228
104619458146194582TC50GENIChomozygous116585230
104619492246194923TG47GENIChomozygous116585232
104619529846195299GT45GENIChomozygous116585234
104619623846196238AAAAC66GENICpossibly homozygous128814166
104619652346196523T29GENICpossibly homozygous128814167
104619657846196582TGTG43GENIChomozygous128814168
104619661046196630TGTGTGTGTGTATCTGTGTG51GENIChomozygous128814169
104619751146197513AG50GENIChomozygous128814170
104619808146198082GC48GENIChomozygous116931244
104620004846200049A50GENIChomozygous128814171
104620111346201114AG65GENIChomozygous116585236
104620286146202861CAGGGCTA42GENIChomozygous128814172
104620373246203733TC48GENIChomozygous116585238
104620481346204814TG49GENIChomozygous116585240
104620516546205166CA54GENIChomozygous117993467
104620516846205168C54GENIChomozygous128814173
104618737246187373AT31GENICheterozygous128869082
104618962446189625AG51GENIChomozygous128869083