chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221272998221272999AG75GENICpossibly homozygous108544244
1221274047221274048TG65GENIChomozygous108544248
1221274064221274065TC65GENIChomozygous108544250
1221274342221274343AG64GENIChomozygous108544252
1221274483221274484AG41GENIChomozygous108544254
1221274534221274535GC39GENIChomozygous108544256
1221274958221274959AT60GENIChomozygous108544258
1221275539221275540TC53GENIChomozygous108544262
1221275615221275616TC62GENIChomozygous108544264
1221275775221275776CT60GENIChomozygous108544266
1221276196221276197TC65GENIChomozygous108544268
1221276268221276269CG49GENIChomozygous108544270
1221276375221276376TA58GENIChomozygous108544272
1221276404221276405AG57GENIChomozygous108544274
1221276519221276520TC67GENIChomozygous108544276
1221276575221276576TG69GENIChomozygous108544278
1221276798221276799AG72GENIChomozygous108544280
1221276857221276858GT66GENIChomozygous108544282
1221277042221277043GA53GENIChomozygous108544284
1221277941221277942GA43GENIChomozygous108544290
1221278159221278160TC76GENIChomozygous108544292
1221278752221278753TC57GENIChomozygous108544294
1221278833221278834AG56GENIChomozygous108544296
1221279106221279107GT58GENIChomozygous108544298
1221279331221279332TC53GENIChomozygous108544300
1221279640221279641AC53GENIChomozygous108544302
1221280984221280985AG51GENIChomozygous108544304
1221275202221275206CCTA60GENIChomozygous127485752
1221275207221275207GAGGTT61GENIChomozygous127485753
1221275393221275397CTGC42GENIChomozygous127485754
1221276165221276165A73GENIChomozygous127485755
1221280307221280307A40GENICpossibly homozygous127485760
1221278903221278906CTT45GENICpossibly homozygous127485757
1221279346221279346A58GENIChomozygous127485758
1221279701221279701A51GENIChomozygous127485759
1221280860221280877ACCTAACCCTAACCCTA68GENIChomozygous127485761
1221276382221276382A61GENIChomozygous129845082
1221276385221276385A60GENIChomozygous131782540
1221277414221277418AAAG55GENIChomozygous131992344