chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134993593134993594CT24GENIChomozygous114144204
5134994072134994073AG23GENIChomozygous114144205
5134994256134994257AG9GENIChomozygous114144206
5134994271134994272GA11GENICheterozygous114144207
5134994483134994484GC10GENIChomozygous114144208
5134994905134994906CA12GENIChomozygous126204564
5134995060134995061AT10GENICheterozygous126239291
5134995071134995072TA12GENICheterozygous126280438
5134996227134996228CG22GENIChomozygous114442330
5134996774134996775CT16GENIChomozygous114144210
5134997446134997447TA5GENIChomozygous126280440
5134997473134997474TC14GENIChomozygous114144212
5134998512134998513TC15GENIChomozygous114144215
5134998629134998630TA26GENIChomozygous114144216
5134998849134998850AG10GENIChomozygous114144217
5134999511134999512GA21GENIChomozygous114144218
5134999643134999644CT13GENIChomozygous114144219
5134999855134999856AG18GENIChomozygous114144220
5135000231135000232CT29GENIChomozygous114144221
5135000463135000464CT4GENIChomozygous126280442
5135000787135000788AT18GENIChomozygous114144222
5135000958135000959AG20GENIChomozygous114017521
5135001224135001225TC12GENIChomozygous114144223
5135001284135001285AG8GENIChomozygous114144224
5135001325135001326GA7GENIChomozygous114144225
5135001359135001360TC7GENIChomozygous114144226