chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141410870514108706AT38GENIChomozygous113351463
141410872114108722GC37GENIChomozygous113807110
141411116214111163AT33GENIChomozygous113575786
141411418314114184GC30GENIChomozygous113659143
141411419314114194TG28GENIChomozygous113659145
141411430214114303AG27GENIChomozygous113351465
141411432114114322GA33GENIChomozygous113718838
141411458414114585GC22GENIChomozygous113659149
141411480814114809AT39GENIChomozygous113659151
141411556114115562CT35GENIChomozygous113659153
141411584814115849CT34GENIChomozygous113659155
141411591014115911CT32GENIChomozygous113659157
141411614414116145AG36GENIChomozygous113659159
141411711314117114GT36GENIChomozygous113659163
141411727314117274AG27GENIChomozygous113659165
141411933914119340AG31GENIChomozygous113659173
141411783614117837AG25GENIChomozygous113659167
141411932414119325TC28GENIChomozygous113659171
141411991214119913GA18GENIChomozygous113807112
141412127514121276AG32GENIChomozygous113351487
141412330414123305AT23GENIChomozygous113659179
141412425014124251GC50GENIChomozygous113807114
141412444414124445AG30GENIChomozygous113659181
141412444714124448GA33GENIChomozygous113807116
141412570014125701CT26GENIChomozygous113659185
141412621114126212CG47GENIChomozygous113807118
141412647514126476TC23GENIChomozygous113807120
141412661314126614AC30GENIChomozygous113807122
141412883614128837AT30GENIChomozygous113807124
141412949614129497GA45GENIChomozygous113807126