chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 205128834 205128835 G A 36 GENIC homozygous 613039691 4 205129264 205129265 A G 38 GENIC homozygous 613039692 4 205129586 205129587 T TG 22 GENIC homozygous 737274830 4 205129782 205129783 T C 35 GENIC homozygous 613039693 4 205129956 205129957 C T 23 GENIC homozygous 613039694 4 205130242 205130243 C T 23 GENIC homozygous 613039695 4 205130304 205130305 C T 17 GENIC homozygous 613039696 4 205130305 205130306 T C 16 GENIC homozygous 613039697 4 205130578 205130579 C T 23 GENIC homozygous 613039698 4 205130927 205130928 C G 35 GENIC homozygous 613039699 4 205131056 205131057 T C 29 GENIC homozygous 613039700 4 205131067 205131068 A G 28 GENIC homozygous 613039701 4 205131439 205131440 G C 29 GENIC homozygous 613039702 4 205132645 205132646 G A 20 GENIC homozygous 613039703 4 205133026 205133027 G A 43 GENIC homozygous 615811901 4 205133039 205133040 A G 40 GENIC homozygous 613039704 4 205133447 205133448 G A 43 GENIC homozygous 613039705 4 205133966 205133967 C T 28 GENIC possibly homozygous 613039706 4 205134011 205134012 T C 33 GENIC homozygous 613039707 4 205134854 205134855 C T 41 GENIC homozygous 613039708 4 205135577 205135578 C T 34 GENIC homozygous 613039709 4 205137912 205137913 C T 2 GENIC homozygous 615811902 4 205138221 205138222 T C 23 GENIC homozygous 613039710 4 205138227 205138228 G GTT 16 GENIC possibly homozygous 737274831 4 205138227 205138228 G GTTT 16 GENIC heterozygous 737274832 4 205149823 205149824 T C 29 GENIC homozygous 613039711 4 205149920 205149921 T A 32 GENIC homozygous 613039712