chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124835435348354354TC37GENIChomozygous115346217
124835436048354361TC38GENIChomozygous115346219
124835436948354370TC36GENIChomozygous115346221
124835437048354371TC36GENIChomozygous115346223
124835437748354378TC40GENIChomozygous115346225
124835438248354383TC39GENIChomozygous115346227
124835438348354384TC38GENIChomozygous115346229
124835469148354692TC28GENIChomozygous115346237
124835991948359920CT28GENIChomozygous115547603
124836051248360513TA12GENIChomozygous115480644
124836116748361168GA23GENIChomozygous115547605
124836139948361400TC21GENIChomozygous115346251
124836178648361787TC29GENIChomozygous115346253
124836186648361867AG22GENIChomozygous115346255
124836199248361993TA29GENIChomozygous115547607
124836326948363270CT13GENIChomozygous115346259
124836328248363283AG13GENIChomozygous115346261
124836359748363598GA21GENIChomozygous115547609
124836390748363908AT14GENIChomozygous115547611
124836474548364746CT26GENIChomozygous115547613
124836700748367008AC42GENIChomozygous115346269
124836700948367010AT43GENIChomozygous115346271
124836726048367261TG18GENIChomozygous115346280
124836734948367350CA3GENIChomozygous115444281
124837001548370016TA5GENIChomozygous115444282
124836276748362768GA20GENIChomozygous115583706
124836418748364188TC19GENIChomozygous115583708