chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109145325291453253GT24GENIChomozygous944683675
109145401791454018AG21GENIChomozygous944683676
109145427991454280TC25GENIChomozygous944683677
109145431891454319AT21GENIChomozygous944683678
109145504291455043CG31GENIChomozygous944683679
109145514591455146CT31GENIChomozygous944683680
109145519991455200AG27GENIChomozygous944683681
109145569791455698GA17GENIChomozygous944683682
109146089391460894CT37GENIChomozygous944683683
109146712991467130TC37GENIChomozygous944683684
109146851291468513AG30GENIChomozygous944683685
109146889991468900AG32GENIChomozygous944683686
109146911791469118CA42GENIChomozygous944683687
109147070591470706CT24GENIChomozygous944683688
109147123691471237CT27GENIChomozygous944683689
109147154091471541CT42GENIChomozygous944683690
109147297791472978CT30GENIChomozygous944683691
109147335491473355TG40GENIChomozygous944683692
109147526891475269CT38GENIChomozygous944683693
109147596891475969AT22GENIChomozygous944683694
109147652991476530CT23GENIChomozygous944683695
109148319691483197TC28GENIChomozygous944683696
109148530091485301CT38GENIChomozygous944683697
109148898891488989TC20GENIChomozygous944683698
109149013591490136CA29GENIChomozygous944683699
109149048491490485CG39GENIChomozygous944683700
109149442091494421CT26GENIChomozygous944683701
109149447991494480GA26GENIChomozygous944683702
109149585291495853TC26GENIChomozygous944683703
109149626091496261AT36GENIChomozygous944683704
109149712891497129GA28GENIChomozygous944683705
109149737791497378AT15GENIChomozygous944683706
109149809391498094TC42GENIChomozygous944683707