chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246043332246043333AG27GENIChomozygous142880493
1246043471246043472CT30GENIChomozygous142880494
1246043485246043486AC32GENIChomozygous142880495
1246044444246044445TC34GENIChomozygous142880496
1246044484246044485TC38GENIChomozygous135855631
1246044505246044506AG38GENIChomozygous142880497
1246044743246044744AG50GENIChomozygous142880498
1246045134246045135TC35GENIChomozygous142880499
1246045573246045574TC28GENIChomozygous135855632
1246046521246046522A6GENICheterozygous404426401
1246046530246046531C7GENICheterozygous404426402
1246046530246046531CG7GENICheterozygous404426403
1246044161246044162AG6GENIChomozygous153917332
1246044161246044162A6GENICheterozygous402984230
1246046521246046522AG5GENIChomozygous145340202
1246046585246046591GAGACA5GENIChomozygous142798173
1246044092246044092GT2GENIChomozygous135470988
1246044137246044137GTGTGTGTGTGTGTATATGTGTCTGTG6GENIChomozygous145250613
1246046494246046496CA16GENIChomozygous145250614
1246046869246046870AC25GENIChomozygous135855635
1246046885246046886TG26GENIChomozygous145340203
1246047373246047374GA30GENIChomozygous145340204
1246047499246047500TC38GENIChomozygous135855637
1246047712246047713A44GENIChomozygous142798175
1246048123246048124TC45GENIChomozygous135855638