chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134993593134993594CT65GENIChomozygous114144204
5134994072134994073AG69GENIChomozygous114144205
5134994256134994257AG49GENIChomozygous114144206
5134994271134994272GA45GENIChomozygous114144207
5134994483134994484GC56GENIChomozygous114144208
5134995393134995394TC54GENICpossibly homozygous114144209
5134996774134996775CT52GENIChomozygous114144210
5134997208134997209AG60GENIChomozygous114144211
5134997473134997474TC66GENIChomozygous114144212
5134997866134997867CT61GENIChomozygous114144213
5134998377134998378GA74GENICpossibly homozygous114144214
5134998512134998513TC42GENIChomozygous114144215
5134998629134998630TA56GENIChomozygous114144216
5134998849134998850AG61GENICpossibly homozygous114144217
5134999511134999512GA58GENIChomozygous114144218
5134999643134999644CT70GENIChomozygous114144219
5134999855134999856AG50GENIChomozygous114144220
5135000231135000232CT69GENIChomozygous114144221
5135000787135000788AT43GENICpossibly homozygous114144222
5135000958135000959AG50GENIChomozygous114017521
5135001224135001225TC44GENIChomozygous114144223
5135001284135001285AG52GENIChomozygous114144224
5135001325135001326GA54GENICpossibly homozygous114144225
5135001359135001360TC49GENIChomozygous114144226