chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 93197958 93197959 G T 15 GENIC homozygous 117388682 9 93205563 93205564 A C 46 GENIC possibly homozygous 117600472 9 93241084 93241085 G T 19 GENIC possibly homozygous 117388712 9 93265704 93265705 C T 31 GENIC homozygous 117388732 9 93270172 93270173 C T 34 GENIC heterozygous 117828922 9 93271520 93271521 T G 21 GENIC homozygous 117388744 9 93271589 93271590 C G 26 GENIC homozygous 117388745 9 93271646 93271647 T G 30 GENIC homozygous 117388747 9 93281996 93281997 A C 30 GENIC heterozygous 117600474 9 93286293 93286294 C A 32 GENIC heterozygous 117388767 9 93286299 93286300 T C 37 GENIC heterozygous 117388768 9 93287680 93287681 G T 24 GENIC heterozygous 117388769 9 93287683 93287684 G T 26 GENIC heterozygous 117388770 9 93292574 93292575 T C 15 GENIC heterozygous 117801029 9 93295595 93295596 T G 40 GENIC homozygous 117388784 9 93298495 93298496 A G 29 GENIC homozygous 117388790 9 93299025 93299026 G A 29 GENIC homozygous 117600476