chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151514188151514196CTCTCTCC7GENIChomozygous127943655
3151514965151514966CT25GENIChomozygous111777670
3151517534151517535AG26GENIChomozygous111777672
3151519183151519183C33GENIChomozygous127943656
3151519994151519995GC16GENIChomozygous111777676
3151520794151520795GA28GENIChomozygous111777678
3151521214151521215CT19GENIChomozygous111777680
3151521853151521854GA24GENIChomozygous111777682
3151522043151522069TGTGTGTGTGTGTGTGTGTGTGCTGC17GENICheterozygous127943657
3151522593151522594A19GENIChomozygous127943658
3151523454151523455AG16GENIChomozygous111777684
3151525264151525265GA17GENICpossibly homozygous111777686
3151525573151525574TG9GENIChomozygous127994361
3151526739151526740TC18GENIChomozygous111777688
3151526931151526932GA18GENIChomozygous111777690
3151527834151527836CC19GENIChomozygous127943659
3151528785151528786AG15GENIChomozygous111777692
3151530256151530257CT23GENIChomozygous111777694
3151531761151531762TC19GENIChomozygous111777696
3151535190151535191AG15GENIChomozygous111777698
3151541015151541016AG26GENIChomozygous111777700
3151543171151543172AG26GENIChomozygous111777702
3151544558151544559GA17GENIChomozygous111777704