chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 42617656 42617657 C T 12 GENIC homozygous 143578706 13 42620080 42620081 G A 34 GENIC homozygous 143578707 13 42620772 42620773 C A 14 GENIC homozygous 141042559 13 42620079 42620079 A 33 GENIC homozygous 143549456 13 42622548 42622549 A G 31 GENIC homozygous 143578708 13 42623526 42623527 G C 34 GENIC homozygous 143578709 13 42623628 42623628 AGAT 36 GENIC homozygous 143549457 13 42625064 42625065 G A 17 GENIC possibly homozygous 143578710 13 42626683 42626684 C A 25 GENIC homozygous 143578711 13 42628194 42628195 A T 20 GENIC homozygous 143578712 13 42628195 42628196 A T 20 GENIC homozygous 143578713 13 42628274 42628275 G A 25 GENIC homozygous 143578714 13 42628488 42628488 CTGGGTG 18 GENIC homozygous 143549458 13 42631545 42631545 CTTAT 22 GENIC homozygous 143549459 13 42632354 42632355 C T 28 GENIC homozygous 143578720 13 42629760 42629761 T C 30 GENIC homozygous 143578715 13 42630397 42630398 T C 28 GENIC homozygous 143578716 13 42630853 42630854 T C 33 GENIC homozygous 143578717 13 42631276 42631277 A C 23 GENIC homozygous 143578718 13 42631789 42631790 A G 31 GENIC homozygous 143578719 13 42634306 42634307 A G 25 GENIC homozygous 143578721 13 42634484 42634485 A G 30 GENIC homozygous 143578722 13 42634952 42634953 C G 22 GENIC homozygous 143578723 13 42635120 42635121 C T 21 GENIC homozygous 143578724 13 42635831 42635832 T C 26 GENIC homozygous 143578725 13 42636700 42636701 G A 15 GENIC homozygous 143578726 13 42636884 42636885 G A 29 GENIC homozygous 143578727