chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3140125785140125785CTTATTTTCTTAT13GENIChomozygous127936233
3140128904140128905TC21GENIChomozygous111752280
3140129544140129545TC20GENIChomozygous111752282
3140130269140130270TC19GENIChomozygous111752288
3140134510140134511A16GENIChomozygous127936237
3140134793140134794GA21GENIChomozygous111752304
3140127857140127860CTT20GENIChomozygous130912094
3140133616140133617T19GENICpossibly homozygous130912095
3140131150140131274AAAAAGATCTGGTTTAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAGACCCAAAAAAAAAAAAAAAAAA4GENICheterozygous129891935
3140130427140130428GA24GENIChomozygous112166935
3140135514140135515TC23GENIChomozygous112166939
3140130181140130182TC18GENIChomozygous112166933
3140132567140132568TC22GENIChomozygous112166937
3140136429140136430GA27GENICpossibly homozygous112166941
3140138823140138824CT16GENIChomozygous112166943
3140139764140139765CT21GENIChomozygous112166945
3140140152140140153CT18GENIChomozygous111752328
3140140169140140170GT17GENIChomozygous111752330
3140141142140141143CA31GENIChomozygous111752334