chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1250560469250560470AT16GENICheterozygous121210397
1250560753250560753A41GENICheterozygous131266075
1250580050250580051GA9GENIChomozygous108608204
1250580074250580074G10GENIChomozygous127503233
1250580086250580086A12GENIChomozygous127503234
1250580102250580103G14GENIChomozygous127503235
1250580112250580113T14GENIChomozygous127503236
1250580145250580145C18GENIChomozygous127503237
1250580168250580169T19GENIChomozygous127503238
1250580176250580177TA17GENIChomozygous120493910
1250580177250580178AT17GENIChomozygous120476873
1250580187250580188A16GENIChomozygous127503239
1250580234250580235C19GENIChomozygous127503240
1250601761250601762CA38GENIChomozygous108608250
1250612556250612558AG34GENICheterozygous130621467
1250579855250579856T2GENIChomozygous132541793
1250596814250596815TA7GENICheterozygous130241514
1250597169250597170CT10GENICheterozygous130241516
1250656699250656700AC38GENIChomozygous108608412
1250658825250658865GTGTCTGTGTGTCTGCGTGTCTGCGTGTCTGCGTGTCTGC19GENIChomozygous132541794