chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 17615986 17615987 T C 22 GENIC homozygous 777096575 14 17617028 17617029 C A 20 GENIC homozygous 777096576 14 17621063 17621064 T C 33 GENIC homozygous 777096577 14 17621382 17621383 T C 44 GENIC homozygous 777096578 14 17622565 17622566 T A 26 GENIC homozygous 777096579 14 17623031 17623032 C T 34 GENIC possibly homozygous 777096580 14 17624364 17624365 C T 52 GENIC homozygous 777096581 14 17624390 17624391 T C 58 GENIC homozygous 777096582 14 17624426 17624427 C G 60 GENIC homozygous 777096583 14 17625885 17625886 A G 26 GENIC homozygous 777096584 14 17629810 17629811 A G 21 GENIC homozygous 777096585 14 17629837 17629838 T C 23 GENIC homozygous 777096586 14 17629841 17629842 T C 22 GENIC homozygous 777096587 14 17629925 17629926 A G 37 GENIC homozygous 777096588 14 17630522 17630523 T A 24 GENIC homozygous 777096589 14 17630650 17630651 T G 16 GENIC homozygous 777096590