chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 17615986 17615987 T C 16 GENIC homozygous 930237728 14 17617028 17617029 C A 17 GENIC homozygous 930237729 14 17621063 17621064 T C 31 GENIC homozygous 930237730 14 17621382 17621383 T C 40 GENIC homozygous 930237731 14 17622565 17622566 T A 24 GENIC homozygous 930237732 14 17623031 17623032 C T 29 GENIC possibly homozygous 930237733 14 17624364 17624365 C T 50 GENIC homozygous 930237734 14 17625885 17625886 A G 23 GENIC homozygous 930237735 14 17629810 17629811 A G 17 GENIC homozygous 930237736 14 17629837 17629838 T C 22 GENIC homozygous 930237737 14 17629841 17629842 T C 21 GENIC homozygous 930237738 14 17629925 17629926 A G 36 GENIC homozygous 930237739 14 17630522 17630523 T A 24 GENIC homozygous 930237740 14 17630650 17630651 T G 16 GENIC homozygous 930237741