chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5171366234171366235TA10GENIChomozygous114091756
5171366237171366238AG9GENIChomozygous114091758
5171366239171366240TG9GENIChomozygous114091760
5171366242171366243TA9GENIChomozygous114091762
5171366245171366246TG9GENIChomozygous114091764
5171366250171366251CA9GENIChomozygous114091766
5171366251171366252TG9GENIChomozygous114091768
5171382753171382754TA34GENICheterozygous114091777
5171382760171382761TA38GENICheterozygous114091779
5171388798171388799CA58GENICheterozygous114091781
5171389481171389482TC51GENIChomozygous114091783
5171389553171389554CT51GENIChomozygous114091785
5171390639171390640TG8GENIChomozygous114652737
5171394293171394294AC58GENIChomozygous114091787
5171394696171394697TG43GENIChomozygous114091789
5171394729171394730TG35GENICpossibly homozygous114091795
5171395100171395101AC72GENICpossibly homozygous114091797
5171396236171396237AC45GENIChomozygous114091799
5171403150171403151TC31GENIChomozygous114091801
5171403151171403152TA31GENIChomozygous114091803
5171403152171403153TC31GENIChomozygous114091805
5171403154171403155TC31GENIChomozygous114091807
5171404766171404767CA26GENICpossibly homozygous114091809
5171405265171405266AG2GENIChomozygous114456385