chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2140543010140543010A35GENIChomozygous127684802
2140543019140543020CA39GENIChomozygous110594492
2140543254140543255TG56GENIChomozygous110035142
2140544416140544417AT37GENIChomozygous110035143
2140545103140545104AG49GENIChomozygous110035145
2140545626140545626T48GENIChomozygous127684803
2140545798140545799AG39GENIChomozygous110035146
2140546550140546551GT25GENIChomozygous110035148
2140547929140547930T48GENICpossibly homozygous127684805
2140548101140548102GA45GENIChomozygous110035149
2140548932140548933TG51GENIChomozygous110035151
2140549073140549075TA44GENIChomozygous127684806
2140549496140549497AG33GENIChomozygous110035152
2140550130140550130A58GENIChomozygous127684807
2140550134140550134A61GENIChomozygous127684808
2140550352140550353GA53GENIChomozygous110035154
2140550800140550801CT53GENIChomozygous110035156
2140551269140551270CG52GENIChomozygous110035157
2140551283140551284CT56GENIChomozygous110035159
2140551310140551311CG56GENIChomozygous110035160
2140551479140551481CT50GENIChomozygous127684809
2140551519140551520TC52GENIChomozygous110035162
2140551563140551564TC41GENIChomozygous110035164
2140551826140551826T37GENICheterozygous127684810
2140552190140552191AG63GENIChomozygous110035165
2140552201140552202AG62GENIChomozygous110035167
2140550131140550132CA60GENIChomozygous120127220