chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 30161084 30161085 A G 54 GENIC homozygous 776814922 12 30164486 30164487 A C 30 GENIC homozygous 776814923 12 30165458 30165459 G T 40 GENIC possibly homozygous 776814924 12 30165889 30165890 G A 53 GENIC homozygous 776814925 12 30166404 30166405 C T 42 GENIC possibly homozygous 776814926 12 30166449 30166450 C T 47 GENIC possibly homozygous 776814927 12 30166464 30166465 C A 53 GENIC homozygous 776814928 12 30167445 30167446 A G 41 GENIC homozygous 776814929 12 30168240 30168241 C A 29 GENIC possibly homozygous 776814930 12 30169455 30169456 C T 23 GENIC homozygous 776814931 12 30170287 30170288 A G 45 GENIC homozygous 776814932 12 30171217 30171218 T C 51 GENIC homozygous 776814933 12 30171243 30171244 G A 46 GENIC homozygous 776814934 12 30171627 30171628 G A 41 GENIC homozygous 776814935 12 30172688 30172689 T G 48 GENIC homozygous 776814936 12 30172829 30172830 A C 65 GENIC homozygous 776814937 12 30173055 30173056 C T 18 GENIC heterozygous 776814938 12 30173065 30173066 C T 19 GENIC heterozygous 776814939 12 30174633 30174634 C T 40 GENIC homozygous 776814940 12 30175005 30175006 G A 53 GENIC homozygous 776814941 12 30175099 30175100 C T 66 GENIC homozygous 776814942 12 30176130 30176131 G A 48 GENIC homozygous 776814943 12 30176322 30176323 T G 56 GENIC homozygous 776814944 12 30177099 30177100 T C 45 GENIC homozygous 776814945 12 30177139 30177140 C T 41 GENIC homozygous 776814946 12 30177201 30177202 T C 55 GENIC homozygous 776814947 12 30177318 30177319 G A 49 GENIC homozygous 776814948 12 30177452 30177453 G C 45 GENIC possibly homozygous 776814949 12 30177454 30177455 T A 45 GENIC homozygous 776814950 12 30177583 30177584 T C 68 GENIC homozygous 776814951