chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4211029158211029159AG28GENIChomozygous57072890
4211029590211029592TT--13GENICheterozygous57611399
4211029591211029592T-13GENICheterozygous57611401
4211030093211030094A-17GENICheterozygous57364523
4211030102211030105CCT---11GENICpossibly homozygous57072892
4211030103211030105CT--13GENIChomozygous57072893
4211030104211030105T-11GENIChomozygous57072894
4211030368211030369CT23GENIChomozygous57611403
4211030677211030678GA34GENIChomozygous57611405
4211030713211030714TC26GENIChomozygous57072898
4211032008211032009TC26GENIChomozygous57072902
4211033354211033355AG24GENIChomozygous57072906
4211033533211033534A-25GENIChomozygous57072907
4211034446211034447CG28GENIChomozygous57072909
4211035531211035532CT26GENIChomozygous57072911
4211036485211036486CCAAAAA6GENIChomozygous57072912
4211037490211037491TC23GENICpossibly homozygous57611407
4211037562211037563CCTT19GENIChomozygous57072914
4211038346211038347CA39GENIChomozygous57611409
4211038353211038354AG38GENIChomozygous57611411
4211038672211038673G-14GENIChomozygous57611413
4211039256211039257CT28GENIChomozygous57611415
4211039802211039803TC22GENIChomozygous57072918