chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
788463198846320CT65GENIChomozygous137999220
788477818847781CTGT62GENIChomozygous137934483
788490498849050AG39GENIChomozygous137999221
788490658849065GAG7GENIChomozygous137934484
788491278849127GG9GENIChomozygous137934485
788491288849128G9GENIChomozygous137934486
788491318849131GAGGAG9GENIChomozygous137934487
788491498849149GAA7GENIChomozygous137934488
788491558849155GAA7GENIChomozygous137934489
788491698849169G3GENIChomozygous137934490
788491718849171AGAGGGGGAGGAGGGGG3GENIChomozygous137934491
788491858849185GAGGAGGAAGAGGAGGAGGAAGAG11GENIChomozygous137934492
788492218849222TC30GENIChomozygous137999222
788499048849905GA66GENIChomozygous137999223
788499318849932GC66GENICpossibly homozygous137999224
788499778849978GC62GENIChomozygous137999225
788499888849989CT61GENIChomozygous137999226
788520348852034CACAGCCGCGGCCCAG55GENIChomozygous137934493
788526008852600AC49GENIChomozygous137934494
788528408852841GA68GENIChomozygous137999231
788510468851047TC65GENIChomozygous137999227
788517858851786AT79GENIChomozygous137999228
788518128851813GT80GENIChomozygous137999229
788526708852671CT40GENIChomozygous137999230
788529168852917AG77GENIChomozygous137999232
788531418853142GT36GENIChomozygous137999233
788537078853709CA48GENIChomozygous137934495
788546638854664TG59GENIChomozygous137999234
788552168855217CA2GENIChomozygous137999235
788554808855481AG65GENIChomozygous137999237
788557888855789CT60GENIChomozygous137999238
788558688855869TC57GENIChomozygous137999239
788559928855993TC71GENIChomozygous137999240