chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91022251410222515CT20GENIChomozygous932704373
91022284210222843CT12GENIChomozygous932704374
91022439010224391CA13GENIChomozygous932704375
91023050210230503AG16GENIChomozygous932704376
91023361210233613TG12GENIChomozygous932704377
91023446010234461AC5GENIChomozygous932704378
91023561510235616GC11GENIChomozygous932704379
91023912110239122AG8GENIChomozygous932704380
91023982010239821TC10GENIChomozygous932704381
91023983310239834GC10GENIChomozygous932704382
91023983510239836GC10GENIChomozygous932704383
91023984210239843AC10GENIChomozygous932704384
91023984510239846AC10GENIChomozygous932704385
91024266110242662AC3GENIChomozygous932704386
91024309810243099TC7GENIChomozygous932704387
91024486110244862AG11GENIChomozygous932704388
91024610910246110GT13GENIChomozygous932704389
91024859510248596CT5GENIChomozygous932704390
91024872610248727CT9GENIChomozygous932704391
91024964710249648TC6GENIChomozygous932704392
91024999610249997CT12GENIChomozygous932704393
91025113810251139CT8GENIChomozygous932704394
91025343810253439GA9GENIChomozygous932704395
91025374710253748AG10GENIChomozygous932704396
91025415110254152CG4GENIChomozygous932704397
91025859510258596GT9GENIChomozygous932704398
91026048710260488CT9GENIChomozygous932704399
91026162810261629GC8GENIChomozygous932704400
91026706410267065AG7GENIChomozygous932704401
91026819110268192GA19GENIChomozygous932704402
91026852410268525AG16GENIChomozygous932704403
91027011610270117TC4GENIChomozygous932704404
91027011810270119GA4GENIChomozygous932704405
91027091810270919CT10GENIChomozygous932704406
91027117910271180TC9GENIChomozygous932704407
91027947210279473TC15GENIChomozygous932704408