chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2147382917147382918TA40GENIChomozygous111265072
2147383035147383036AT48GENIChomozygous110046121
2147384511147384512AG42GENIChomozygous111265074
2147384840147384841GA41GENIChomozygous111265076
2147385325147385326AG49GENIChomozygous110046123
2147385784147385785CT41GENIChomozygous111265078
2147383545147383545A37GENICpossibly homozygous127688277
2147386653147386654C32GENIChomozygous127688278
2147387638147387639AT33GENIChomozygous110046124
2147387787147387788TC44GENIChomozygous110046126
2147390892147390893TC16GENIChomozygous110046128
2147391746147391747TG39GENIChomozygous110046129