chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257786500257786501GA57GENIChomozygous120385167
2257786543257786544AG58GENIChomozygous111044144
2257786713257786714AG48GENICpossibly homozygous111044146
2257786778257786779GA84GENIChomozygous111044148
2257787741257787742TC22GENIChomozygous111044150
2257787744257787745TA24GENIChomozygous111044152
2257787818257787819AG39GENIChomozygous111044156
2257788935257788936GA47GENIChomozygous111044182
2257788996257788997CG50GENIChomozygous111044184
2257789080257789081TA33GENIChomozygous111044186
2257789097257789098AG37GENIChomozygous111044188
2257789100257789101CT37GENIChomozygous111044190
2257789109257789110CT35GENIChomozygous111044192
2257789112257789113AG36GENIChomozygous111044194
2257789174257789175GA46GENIChomozygous111044196
2257789378257789379GA20GENIChomozygous111044204
2257789643257789644CG27GENIChomozygous111044206
2257789654257789655AC31GENIChomozygous111044208
2257789912257789913TC49GENIChomozygous110412682
2257788403257788404AG51GENIChomozygous110412678
2257790037257790038AC37GENIChomozygous110412684
2257790124257790125TC42GENIChomozygous111044210
2257790333257790334GA34GENIChomozygous111044212
2257790420257790421TC24GENIChomozygous111044214
2257790505257790506TC15GENIChomozygous110412690
2257790794257790795CT32GENIChomozygous111044216
2257790804257790805AG31GENIChomozygous111044218
2257790820257790821GA32GENIChomozygous111044220
2257790937257790938AG16GENIChomozygous111044222
2257790946257790947GA14GENIChomozygous111044224
2257791202257791203CT24GENIChomozygous120385168
2257791241257791242GA35GENIChomozygous110412692