chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 130263548 130263678 AAAAATATTTAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAA 27 GENIC homozygous 128520266 7 130263869 130263870 T C 49 GENIC homozygous 115889669 7 130264001 130264030 GGAGGACAGTCCTATGTGTATTGTGTGAG 34 GENIC homozygous 128520267 7 130264554 130264555 C T 45 GENIC homozygous 115889677 7 130265055 130265056 T C 57 GENIC homozygous 115889679 7 130265966 130265981 AAAACAAAGTTGACT 43 GENIC homozygous 128520268 7 130266609 130266610 T C 61 GENIC homozygous 115889681 7 130267073 130267074 A T 56 GENIC homozygous 115889683 7 130267182 130267183 G C 47 GENIC homozygous 115889685 7 130267217 130267218 C T 44 GENIC homozygous 115889687 7 130267486 130267487 A C 64 GENIC possibly homozygous 115889689 7 130267498 130267499 T C 60 GENIC homozygous 115889692 7 130268656 130268657 C T 51 GENIC homozygous 115889694 7 130268681 130268682 T C 48 GENIC homozygous 115889696 7 130270754 130270755 T C 49 GENIC homozygous 115889698 7 130271225 130271229 AGAT 46 GENIC homozygous 128520269 7 130271482 130271482 A 50 GENIC homozygous 128520270 7 130271916 130271917 T C 68 GENIC homozygous 115889700 7 130272607 130272608 T C 64 GENIC homozygous 115889702 7 130273416 130273417 G A 61 GENIC homozygous 115889704 7 130274101 130274102 A G 59 GENIC homozygous 115889706 7 130277368 130277377 AAGCAACAT 55 GENIC homozygous 128520271 7 130284801 130284802 C T 63 GENIC homozygous 115889708 7 130285606 130285607 A G 51 GENIC homozygous 115889710 7 130286818 130286819 C A 51 GENIC homozygous 115889712 7 130287675 130287676 C T 61 GENIC possibly homozygous 115889714