chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 33572846 33572847 G A 20 GENIC homozygous 976988609 14 33573049 33573050 G A 27 GENIC homozygous 976988610 14 33573318 33573319 T G 33 GENIC homozygous 976988611 14 33573789 33573790 C T 20 GENIC homozygous 976988612 14 33573812 33573813 A G 15 GENIC homozygous 976988613 14 33573897 33573898 G A 14 GENIC homozygous 976988614 14 33574099 33574100 A G 27 GENIC homozygous 976988615 14 33574359 33574360 A G 27 GENIC homozygous 976988616 14 33574511 33574512 T C 29 GENIC homozygous 976988617 14 33574645 33574646 A G 30 GENIC homozygous 976988618 14 33574924 33574925 C T 21 GENIC homozygous 976988619 14 33575634 33575635 C T 18 GENIC homozygous 976988620 14 33576070 33576071 A G 34 GENIC homozygous 976988621 14 33576111 33576112 T C 33 GENIC homozygous 976988622 14 33578885 33578886 C G 25 GENIC homozygous 976988623 14 33579113 33579114 A G 19 GENIC homozygous 976988624 14 33579511 33579512 C T 24 GENIC homozygous 976988625 14 33579543 33579544 C A 27 GENIC homozygous 976988626 14 33580028 33580029 A G 20 GENIC homozygous 976988627 14 33580207 33580208 T A 11 GENIC homozygous 976988628 14 33580214 33580215 A G 10 GENIC homozygous 976988629 14 33580554 33580555 A G 4 GENIC homozygous 976988630