chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 80384997 80384998 T C 16 GENIC homozygous 109874610 2 80386842 80386843 C T 17 GENIC homozygous 109874612 2 80390658 80390659 G A 23 GENIC homozygous 109874616 2 80391198 80391199 G A 12 GENIC homozygous 109874618 2 80393656 80393657 C T 4 GENIC homozygous 109874620 2 80394350 80394351 T G 21 GENIC homozygous 109874622 2 80395811 80395812 C T 17 GENIC homozygous 109874624 2 80399557 80399558 A G 20 GENIC homozygous 109874630 2 80402672 80402673 C T 11 GENIC homozygous 109874632 2 80391661 80391662 T A 6 GENIC heterozygous 125574014 2 80403980 80403981 G A 12 GENIC homozygous 109874634 2 80404628 80404629 C T 19 GENIC homozygous 109874636 2 80405003 80405004 C T 17 GENIC homozygous 109874638 2 80405329 80405330 C T 18 GENIC homozygous 109874640 2 80405546 80405547 A G 19 GENIC homozygous 109874642 2 80405724 80405725 T C 28 GENIC heterozygous 109874644 2 80406445 80406446 A G 24 GENIC homozygous 109874646 2 80407028 80407029 C G 17 GENIC homozygous 109874648 2 80407372 80407373 T G 6 GENIC homozygous 109874650 2 80407452 80407453 T C 13 GENIC homozygous 109874652 2 80407845 80407846 T G 18 GENIC homozygous 109874654 2 80405601 80405602 T G 11 GENIC heterozygous 110566966