chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133982065133982066AG22GENIChomozygous114015232
5133984097133984098CT20GENIChomozygous126238937
5133984288133984289CT24GENICheterozygous114015235
5133984371133984372GC17GENICheterozygous114015236
5133984486133984487GA9GENIChomozygous114532377
5133984633133984634TC7GENIChomozygous126238938
5133984788133984789CT4GENIChomozygous126203911
5133984804133984805GA2GENIChomozygous126238939
5133989913133989914TC15GENIChomozygous114015239
5133991146133991147TC20GENIChomozygous114015241
5133992431133992432GT18GENIChomozygous126238959
5133992624133992625GT27GENIChomozygous114015242
5133993004133993005AG12GENIChomozygous126238960
5133994934133994935TC18GENIChomozygous114532401
5133995879133995880AG14GENIChomozygous114015250
5133997605133997606AC15GENIChomozygous126238961
5133998633133998634AG19GENIChomozygous126238963
5134002244134002245AG18GENIChomozygous114015263
5134002410134002411TC32GENIChomozygous126238964
5134002993134002994CG14GENIChomozygous114015264
5134003473134003474GC7GENIChomozygous128300303
5134004039134004040AC15GENIChomozygous126238966
5134005046134005047CT22GENIChomozygous114015265
5134005868134005869TC10GENIChomozygous114015266
5134006156134006157GT14GENIChomozygous130971678
5134006730134006731GA12GENIChomozygous114015267
5134007807134007808AG20GENIChomozygous114015268
5134007872134007873TA26GENIChomozygous114015269
5134007877134007878GA25GENIChomozygous114015270
5134008118134008119GA17GENIChomozygous126238969
5134008164134008165AG18GENIChomozygous119017885
5134008165134008166GC18GENIChomozygous114015272
5134008209134008210GA16GENIChomozygous114015273
5134001899134001900A18GENIChomozygous130962529
5134003470134003470GGGGATTTAGCTCAGTGGTAGAGCGCTTG5GENIChomozygous128241382
5134003472134003472TA7GENIChomozygous128241383
5134003476134003476GC7GENIChomozygous128241384