chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6127408092127408093TC21GENICheterozygous114983228
6127410140127410141AG15GENIChomozygous114983229
6127411780127411781CT16GENIChomozygous114983230
6127419435127419436GT18GENIChomozygous114983231
6127422379127422380AG5GENIChomozygous126420626
6127426021127426022AG5GENICheterozygous114983232
6127432470127432471TC8GENICheterozygous114983234
6127434774127434775AG21GENIChomozygous114983235
6127438618127438619AG29GENIChomozygous114983236
6127490043127490044CT7GENIChomozygous114983325
6127490446127490447CA17GENIChomozygous114983326
6127490650127490651CA19GENIChomozygous114983327
6127490723127490724AG16GENIChomozygous114983328
6127491649127491650TC12GENIChomozygous114983330
6127492457127492458TC13GENIChomozygous114983331
6127493423127493424GA17GENIChomozygous114983332
6127493503127493504GA20GENIChomozygous114983333
6127493657127493658GA10GENIChomozygous114983334
6127493715127493716GA16GENIChomozygous114983335
6127493748127493749GA8GENIChomozygous114983336
6127494692127494693GA13GENIChomozygous114983337
6127494708127494709AG17GENIChomozygous114983338
6127495596127495597TC15GENIChomozygous114983339
6127495701127495702GA8GENICheterozygous114983340
6127496173127496174CT13GENIChomozygous114983341
6127493149127493150TG14GENIChomozygous126365642
6127493239127493240TG14GENIChomozygous126365644
6127493434127493435AG21GENIChomozygous126365646