chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1137607971137607994GAATGTTATGGGAGCCAGCCCCT66GENICpossibly homozygous135431604
1137608114137608115TC81GENIChomozygous135677914
1137609860137609860A48GENICpossibly homozygous135431605
1137609900137609901T56GENIChomozygous135431606
1137610560137610561AG59GENICpossibly homozygous135677915
1137611829137611830AT52GENIChomozygous135677916
1137612751137612752GA64GENIChomozygous135677917
1137614135137614136GA69GENIChomozygous135677918
1137614154137614155AG71GENIChomozygous135677919
1137614609137614610AC42GENIChomozygous135677920
1137614612137614613GA43GENIChomozygous135677921
1137614699137614700CT54GENIChomozygous135677922
1137615731137615732CA55GENICpossibly homozygous135677923