chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94019713 94019714 A G 54 GENIC homozygous 142175879 9 94020419 94020420 A G 61 GENIC homozygous 138630426 9 94022193 94022193 TAA 76 GENIC homozygous 138474478 9 94022364 94022365 G A 66 GENIC homozygous 143420789 9 94022997 94022998 A G 75 GENIC homozygous 138630427 9 94024782 94024782 ATGAGACACT 54 GENIC homozygous 138474479 9 94028043 94028044 G A 58 GENIC homozygous 143420790 9 94030135 94030136 T C 56 GENIC homozygous 142175881 9 94031964 94031965 A C 68 GENIC homozygous 138630428 9 94034535 94034536 C 63 GENIC homozygous 138474480 9 94036211 94036212 C G 53 GENIC homozygous 143420791 9 94037462 94037465 ACT 51 GENIC homozygous 138474481 9 94037468 94037500 AAATGTTAAATATGTTAAATGTTAAATGTTAA 53 GENIC homozygous 138474482 9 94038714 94038715 G C 57 GENIC homozygous 138630431 9 94040257 94040257 A 62 GENIC possibly homozygous 143400451 9 94024274 94024306 CCATACATACATGCACAGGATCTGGGTCAGAT 26 GENIC homozygous 143400448 9 94034191 94034192 T 76 GENIC possibly homozygous 143400449 9 94036213 94036213 A 53 GENIC homozygous 143400450 9 94027006 94027006 ATAG 33 GENIC homozygous 140899643 9 94042539 94042540 G T 54 GENIC homozygous 143420792 9 94044758 94044759 T C 69 GENIC homozygous 138630432 9 94046936 94046936 T 43 GENIC possibly homozygous 142119053 9 94047117 94047233 CGAACCCAGGGCCTTGTGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACTGATATTTTTTTCTTTTCTTTTCTTTTCTTTTTTTTTTTTCCTTCGGAGCTGGGGAT 17 GENIC homozygous 143400452 9 94051380 94051381 T C 64 GENIC possibly homozygous 143420793