chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 17615986 17615987 T C 33 GENIC homozygous 791150114 14 17617028 17617029 C A 8 GENIC homozygous 791150115 14 17621063 17621064 T C 15 GENIC homozygous 791150116 14 17621382 17621383 T C 19 GENIC homozygous 791150117 14 17622565 17622566 T A 15 GENIC homozygous 791150118 14 17623031 17623032 C T 15 GENIC homozygous 791150119 14 17624364 17624365 C T 24 GENIC homozygous 791150120 14 17624390 17624391 T C 24 GENIC homozygous 791150121 14 17624426 17624427 C G 17 GENIC possibly homozygous 791150122 14 17625885 17625886 A G 10 GENIC homozygous 791150123 14 17629810 17629811 A G 20 GENIC homozygous 791150124 14 17629837 17629838 T C 16 GENIC possibly homozygous 791150125 14 17629841 17629842 T C 17 GENIC homozygous 791150126 14 17629925 17629926 A G 18 GENIC homozygous 791150127 14 17630522 17630523 T A 9 GENIC homozygous 791150128 14 17630650 17630651 T G 4 GENIC homozygous 791150129