chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87684882976848830CG18GENIChomozygous116970063
87684898176848982AG16GENIChomozygous116970064
87684959876849604ATATAT15GENIChomozygous131049672
87684998776849988AG11GENIChomozygous116970068
87685016876850169GA21GENIChomozygous116970069
87685033276850333AG12GENIChomozygous116970070
87685037576850376CT13GENIChomozygous116970071
87685084876850848C16GENICpossibly homozygous131049673
87685107176851071C18GENIChomozygous128604398
87685087076850870T15GENIChomozygous128604395
87685091776850918T14GENIChomozygous128604396
87685095376850954G16GENIChomozygous128604397
87685088376850884TG14GENIChomozygous116844447
87685088476850885CT14GENIChomozygous116844448
87685112876851128T13GENIChomozygous128604399
87685113676851137T12GENIChomozygous128604400
87685116976851169G5GENIChomozygous128604401
87685124276851242A5GENIChomozygous128604403
87685129076851291GA12GENIChomozygous116970072
87685134176851342GC15GENIChomozygous116970073
87685143176851432AG24GENIChomozygous116970074
87685152276851522A18GENIChomozygous128604404
87685159976851599T11GENIChomozygous128604405
87685164976851649C12GENIChomozygous128604406
87685165476851654A10GENIChomozygous128604407
87685165676851656A10GENIChomozygous131049674
87685171176851712TC15GENIChomozygous116970075
87685185876851858CA5GENICheterozygous132122963
87685226276852262AGCCC15GENIChomozygous131049675
87685232176852322GT16GENIChomozygous116970076
87685232376852324AG16GENIChomozygous116970077
87685238276852383AT17GENIChomozygous116970078
87685246676852466C18GENIChomozygous131049676
87685494076854940C14GENIChomozygous131049677
87685521576855216CT11GENIChomozygous116970082
87685289376852894TA13GENIChomozygous116970079
87685467776854678CT11GENIChomozygous116970080
87685512476855125CT8GENIChomozygous116970081
87685525376855255TA17GENIChomozygous131049678
87685525776855261CGCC17GENIChomozygous131049679
87685529576855295CC16GENICheterozygous132994663