chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
628122762812277TA73GENIChomozygous115036972
628122782812279AT72GENIChomozygous115036973
628123452812346CT58GENIChomozygous115036974
628186292818630AG92GENICheterozygous114705744
628186882818689GA68GENICheterozygous114705745
628186892818690GC64GENICheterozygous114705746
628186982818699AC63GENICheterozygous114705747
628195892819590CT34GENICpossibly homozygous115036975
628195952819596CG31GENIChomozygous115036976
628195992819600AT29GENIChomozygous115036977
628196372819638CG18GENIChomozygous115036978
628196602819661CG24GENIChomozygous114705748
628196722819673TA31GENIChomozygous115036979
628196792819680CT30GENIChomozygous114705749
628196822819683CT29GENIChomozygous114705750
628196912819692CT33GENIChomozygous114705751
628197032819704CT35GENIChomozygous114705752
628262782826279GT122GENICheterozygous114705758
628263372826338GA101GENICheterozygous114705760
628284922828493CT71GENIChomozygous114705773
628344272834428GT67GENIChomozygous114705786