chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 205128834 205128835 G A 36 GENIC homozygous 506630011 4 205129264 205129265 A G 39 GENIC homozygous 506630012 4 205129586 205129587 T TG 56 GENIC homozygous 685576684 4 205129782 205129783 T C 67 GENIC homozygous 506630013 4 205129956 205129957 C T 44 GENIC possibly homozygous 506630014 4 205130242 205130243 C T 46 GENIC homozygous 506630015 4 205130304 205130305 C T 56 GENIC homozygous 506630016 4 205130305 205130306 T C 55 GENIC homozygous 506630017 4 205130578 205130579 C T 74 GENIC homozygous 506630018 4 205130927 205130928 C G 70 GENIC homozygous 506630019 4 205131056 205131057 T C 41 GENIC homozygous 506630020 4 205131067 205131068 A G 42 GENIC homozygous 506630021 4 205131439 205131440 G C 89 GENIC homozygous 506630022 4 205132645 205132646 G A 49 GENIC homozygous 506630023 4 205133026 205133027 G A 73 GENIC homozygous 510248755 4 205133039 205133040 A G 74 GENIC homozygous 506630024 4 205133447 205133448 G A 49 GENIC homozygous 506630025 4 205133966 205133967 C T 54 GENIC homozygous 506630026 4 205134011 205134012 T C 54 GENIC homozygous 506630027 4 205134854 205134855 C T 82 GENIC homozygous 506630028 4 205135577 205135578 C T 64 GENIC homozygous 506630029 4 205137895 205137896 A ATAAG 10 GENIC homozygous 685576685 4 205138221 205138222 T C 58 GENIC homozygous 506630030 4 205138227 205138228 G GTT 45 GENIC homozygous 685576687 4 205149823 205149824 T C 69 GENIC homozygous 506630031 4 205149920 205149921 T A 73 GENIC possibly homozygous 506630032