chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105428284054282841GA51GENIChomozygous142247995
105428386954283870GA55GENIChomozygous142247996
105428511154285111A58GENIChomozygous142203410
105428511354285114CG59GENIChomozygous142247997
105428537754285378AG56GENIChomozygous142247998
105428676854286769A46GENICpossibly homozygous142203411
105428725554287255GT43GENIChomozygous142203412
105428731554287318AAG14GENICheterozygous142203414
105428905654289057GA61GENIChomozygous142247999
105429113654291137GA47GENIChomozygous142248000
105429140954291410AT71GENIChomozygous142248001
105429345954293460TC41GENIChomozygous142248002
105429392354293923AT41GENIChomozygous142203415
105429415154294155GGGA11GENIChomozygous142203416
105429507354295074AT71GENIChomozygous142248003
105429921554299215C40GENIChomozygous142203417
105428929354289294CT60GENIChomozygous147578608
105429380954293811GG13GENICheterozygous141119107
105429382154293822GC13GENICheterozygous138793220
105429630954296309T30GENIChomozygous143431903