chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104618405746184058CA49GENICpossibly homozygous116585212
104618457846184578T39GENIChomozygous128814161
104618469746184698CT48GENIChomozygous116585214
104618500246185003CT63GENIChomozygous116585216
104618503546185036AG61GENIChomozygous116585218
104618538346185384AG41GENIChomozygous117410415
104618575046185751TC46GENIChomozygous116585220
104618598046185981CT35GENIChomozygous117129048
104618741246187413CA39GENIChomozygous116585222
104618848946188491CA33GENIChomozygous128814163
104618960846189609AG59GENIChomozygous123441210
104618961446189615AG56GENIChomozygous123441211
104618962046189621AG56GENIChomozygous123441212
104618962446189625AG55GENIChomozygous128869083
104618962646189627AG51GENIChomozygous116585224
104618963146189633TA50GENIChomozygous128814164
104618971346189721TATATGTG40GENIChomozygous128814165
104619051546190516TC58GENIChomozygous116585226
104619241646192417TG52GENIChomozygous116585228
104619458146194582TC49GENIChomozygous116585230
104619492246194923TG59GENIChomozygous116585232
104619529846195299GT54GENIChomozygous116585234
104619623846196238AAAAC55GENIChomozygous128814166
104619652346196523T36GENICheterozygous128814167
104619657846196582TGTG40GENIChomozygous128814168
104619661046196630TGTGTGTGTGTATCTGTGTG41GENIChomozygous128814169
104619751146197513AG56GENICpossibly homozygous128814170
104620004846200049A58GENIChomozygous128814171
104620111346201114AG51GENIChomozygous116585236
104620286146202861CAGGGCTA43GENIChomozygous128814172
104620373246203733TC55GENIChomozygous116585238
104620481346204814TG53GENIChomozygous116585240
104620516546205166CA52GENIChomozygous117993467
104620516846205168C52GENIChomozygous128814173
104619808146198082GC54GENIChomozygous116931244