chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 16663258 16663259 C T 12 GENIC homozygous 139094901 12 16663280 16663280 CT 14 GENIC homozygous 139043378 12 16663758 16663759 C T 51 GENIC homozygous 139094902 12 16663770 16663771 G A 54 GENIC homozygous 139094903 12 16663860 16663861 T C 52 GENIC homozygous 139094904 12 16664184 16664185 A G 58 GENIC homozygous 139094905 12 16664225 16664226 G A 53 GENIC homozygous 139094906 12 16665044 16665045 T C 43 GENIC homozygous 139094907 12 16665102 16665102 T 39 GENIC homozygous 139043379 12 16665433 16665433 AAAAA 39 GENIC homozygous 139043380 12 16665728 16665734 TAGGTT 30 GENIC homozygous 139043381 12 16666141 16666142 C 29 GENIC homozygous 139043382 12 16666620 16666621 T C 37 GENIC homozygous 139094908 12 16666814 16666815 C T 38 GENIC homozygous 139094909 12 16667636 16667637 A T 62 GENIC possibly homozygous 139094910 12 16668238 16668239 T C 47 GENIC homozygous 139094911 12 16668868 16668869 C T 52 GENIC homozygous 139094912 12 16669012 16669012 T 43 GENIC possibly homozygous 139043383 12 16669511 16669512 G A 28 GENIC homozygous 139094913 12 16669943 16669944 G T 31 GENIC possibly homozygous 139094914