chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2184172335184172336TC39GENIChomozygous136405204
2184173201184173201TG38GENIChomozygous135966383
2184173652184173653TC55GENIChomozygous136405206
2184173836184173837GA57GENIChomozygous136405207
2184174055184174056GA51GENIChomozygous136405208
2184174389184174389T50GENIChomozygous135966384
2184175146184175147TC47GENIChomozygous136405209
2184175713184175714CT43GENIChomozygous141423353
2184176076184176077AG54GENIChomozygous136405210
2184176334184176335CT53GENIChomozygous136405211
2184176642184176643AG45GENIChomozygous136405212
2184177242184177243AC25GENIChomozygous136405213
2184177261184177262GA18GENIChomozygous136405214
2184177366184177367TC33GENIChomozygous136405215
2184178078184178079GA55GENIChomozygous136405217
2184178104184178104A42GENIChomozygous135966385
2184178158184178159TC31GENIChomozygous136405218
2184178178184178179CT38GENIChomozygous136405219
2184178224184178225TG51GENIChomozygous136405220
2184178556184178557AG47GENIChomozygous136405221
2184178623184178624T41GENIChomozygous135966386
2184178733184178734GA44GENIChomozygous141423354
2184178873184178874CT55GENIChomozygous136405222
2184179070184179071CT34GENIChomozygous136405223
2184179102184179103CT36GENIChomozygous136405224
2184179699184179700CT45GENIChomozygous136405226
2184179725184179725T47GENICpossibly homozygous135966387
2184179836184179837TG50GENIChomozygous136405228
2184179861184179862AG49GENIChomozygous136405229
2184180511184180512AG35GENIChomozygous136405230
2184180758184180759TC18GENIChomozygous136405231
2184179912184179926CTTGATGACAGTGC42GENIChomozygous141334529