chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7133862401133862402TG34GENIChomozygous54125378
7133863887133863888GA19GENIChomozygous54125379
7133864071133864082CACACACACAC-----------8GENICheterozygous54125380
7133864071133864084CACACACACACAC-------------8GENICheterozygous55220896
7133864121133864130GCACAGGAA---------9GENIChomozygous54125381
7133864249133864250GA21GENICpossibly homozygous54125382
7133864577133864578TC31GENIChomozygous54125383
7133865015133865029ATATACATATATAT--------------2GENICheterozygous55281038
7133865017133865029ATACATATATAT------------2GENICheterozygous55281040
7133865446133865447GT32GENIChomozygous54125385
7133865493133865494CA26GENIChomozygous54125386
7133865867133865868TA19GENIChomozygous54125387
7133865896133865897GA22GENIChomozygous54125388
7133865951133865952CCTTT19GENICheterozygous55679508
7133865961133865962CCTTT23GENICpossibly homozygous54125389
7133865961133865962CCTT23GENICheterozygous55362640
7133866058133866059GT18GENIChomozygous54125391
7133866062133866063CT15GENIChomozygous54125392
7133866171133866172CG22GENIChomozygous54125393
7133866189133866190T-26GENIChomozygous54125394
7133866266133866267AAT18GENIChomozygous54125395
7133866345133866346G-19GENIChomozygous54125396
7133866399133866400CG22GENIChomozygous54125397
7133866400133866401AG21GENIChomozygous54125398