chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 58326962 58326963 A G 28 GENIC homozygous 110475906 18 58328601 58328602 C T 20 GENIC homozygous 110475908 18 58328645 58328646 C T 29 GENIC homozygous 110475910 18 58330352 58330353 G A 44 GENIC homozygous 110475911 18 58330901 58330902 T C 21 GENIC homozygous 110475913 18 58332783 58332784 A C 26 GENIC homozygous 110475915 18 58332958 58332959 C G 31 GENIC homozygous 110475917 18 58333058 58333059 G A 32 GENIC homozygous 110475919 18 58333208 58333209 T C 27 GENIC homozygous 110475921 18 58334124 58334125 G A 32 GENIC homozygous 110475923 18 58334464 58334465 C T 28 GENIC homozygous 110475925 18 58334588 58334589 G A 19 GENIC homozygous 110475927 18 58334823 58334824 G A 25 GENIC homozygous 110475929 18 58335335 58335336 T C 26 GENIC homozygous 110475931 18 58335755 58335756 T C 23 GENIC homozygous 110475933 18 58336439 58336440 A G 31 GENIC possibly homozygous 110475935 18 58336690 58336691 C A 17 GENIC homozygous 110475937 18 58336775 58336776 A T 27 GENIC homozygous 110475939 18 58342533 58342534 G A 22 GENIC homozygous 110475941 18 58343002 58343003 T G 28 GENIC homozygous 110475943