chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13109714477109714478CT25GENIChomozygous786775633
13109714746109714747TC17GENIChomozygous786775634
13109715880109715881AG16GENICpossibly homozygous786775635
13109716498109716499CT28GENIChomozygous786775636
13109716773109716774CG27GENIChomozygous786775637
13109718665109718666AC28GENIChomozygous786775638
13109719342109719343TC23GENIChomozygous786775639
13109720457109720458AG25GENIChomozygous786775640
13109721234109721235TC21GENIChomozygous786775641
13109721261109721262AG17GENIChomozygous786775642
13109721497109721498CT20GENIChomozygous786775643
13109725114109725115TC20GENIChomozygous786775644
13109725273109725274TG23GENIChomozygous786775645
13109725443109725444CT23GENIChomozygous786775646
13109726218109726219AT20GENIChomozygous786775647