chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 26346856 26346857 A G 28 GENIC homozygous 50147602 12 26347656 26347657 C CAAAAA 2 GENIC heterozygous 50539336 12 26348757 26348759 AA -- 14 GENIC heterozygous 50539337 12 26348758 26348759 A - 14 GENIC possibly homozygous 50539338 12 26348945 26348946 C T 35 GENIC homozygous 50298905 12 26350320 26350321 C A 33 GENIC homozygous 50298907 12 26351040 26351041 A AT 21 GENIC homozygous 50298909 12 26351335 26351336 G GGAAAGAAAAGAAA 4 GENIC homozygous 50927739 12 26352009 26352010 G A 29 GENIC homozygous 50298919 12 26352894 26352895 C T 26 GENIC homozygous 50298921 12 26353145 26353146 A - 17 GENIC homozygous 50485104 12 26355634 26355635 C A 18 GENIC possibly homozygous 50147620 12 26355636 26355637 C CAAA 9 GENIC possibly homozygous 50539339 12 26355964 26355965 T C 29 GENIC homozygous 50147624 12 26356085 26356086 A G 13 GENIC homozygous 50147626 12 26356354 26356355 C CT 11 GENIC homozygous 50298923 12 26356718 26356719 C G 22 GENIC homozygous 50147628 12 26357237 26357238 T TTTTATTTA 2 GENIC homozygous 50557817 12 26357307 26357309 GT -- 4 GENIC homozygous 50562147 12 26358764 26358765 T C 24 GENIC homozygous 50147648 12 26359997 26359998 A AT 28 GENIC homozygous 50147664 12 26360029 26360030 A G 28 GENIC homozygous 50147666 12 26360536 26360537 G A 11 GENIC homozygous 50298925 12 26361280 26361281 G GT 14 GENIC possibly homozygous 50147682 12 26361356 26361357 A AT 26 GENIC homozygous 50298929 12 26361402 26361403 T TGCGCGC 3 GENIC homozygous 50298933 12 26361782 26361783 T G 13 GENIC possibly homozygous 50927742 12 26361971 26361972 T - 19 GENIC heterozygous 50298937 12 26362451 26362452 C T 39 GENIC homozygous 50298939 12 26362516 26362517 G A 29 GENIC homozygous 50298941