chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167057828170578282CA17GENIChomozygous47691620
167057849870578500GG--15GENIChomozygous47691621
167057914470579145GA15GENIChomozygous47864051
167057960070579628CTCCTCCATCTCTCTCTGCACTGCATCC----------------------------29GENICpossibly homozygous47908913
167058112370581124CT19GENIChomozygous47864061
167058156870581569AG21GENIChomozygous47691631
167058637470586375AAGATT19GENIChomozygous47511552
167058647670586477CCA5GENICheterozygous47934426
167058775170587752AG20GENIChomozygous47511553
167058784070587841CG25GENICpossibly homozygous47511554
167058787470587875CA26GENIChomozygous47511555
167059380270593803AG21GENIChomozygous47511556
167059386370593864TC13GENIChomozygous47511560
167059588770595888CCA4GENICheterozygous47773005
167059725270597253TC29GENICheterozygous47511562
167059734870597349TA30GENICheterozygous47511563
167059739070597391GA39GENICheterozygous47511564
167058647770586478A-5GENICheterozygous47961245
167061355970613560CCT13GENICheterozygous47773006
167061750070617501CA15GENIChomozygous48116371
167062234870622349CCT1GENIChomozygous47961246
167062414370624144CT13GENIChomozygous47511571
167062415070624151CT12GENIChomozygous47511572
167062415370624154CG12GENIChomozygous47511573
167062418670624187CG7GENIChomozygous47511577
167062419070624191CG4GENIChomozygous47511578
167062419270624193CG4GENIChomozygous47511579
167062419670624197CG3GENIChomozygous47511580
167062420870624210CC--2GENIChomozygous47511581
167062421870624226CCCCCACC--------6GENIChomozygous47511582
167062422670624227CG6GENIChomozygous47961247
167062422970624230C-6GENIChomozygous47934435
167062705870627059A-8GENICheterozygous47820703
167064254170642542AG15GENIChomozygous47511584
167064297470642978TGTG----6GENICheterozygous47691718
167064728670647287C-11GENIChomozygous47511587
167064996970649970TTA1GENIChomozygous47934442