chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 46485711 46485712 T G 22 GENIC homozygous 637811540 6 46485907 46485908 A T 22 GENIC homozygous 637811541 6 46486115 46486116 T TC 11 GENIC homozygous 749598701 6 46486543 46486544 G C 17 GENIC homozygous 637811542 6 46487298 46487299 C T 39 GENIC homozygous 637811543 6 46487401 46487402 C T 28 GENIC homozygous 637811544 6 46487709 46487710 C CT 14 GENIC possibly homozygous 749598703 6 46487787 46487788 A G 22 GENIC homozygous 637811545 6 46487854 46487855 G - 18 GENIC homozygous 749598704 6 46488137 46488138 A ACGCG 28 GENIC homozygous 749598705 6 46488142 46488143 C T 23 GENIC homozygous 637811546 6 46488589 46488590 A G 23 GENIC homozygous 637811547 6 46488649 46488650 C G 21 GENIC homozygous 637811548 6 46488701 46488702 T C 20 GENIC homozygous 637811549 6 46488948 46488949 G A 27 GENIC homozygous 637811550 6 46489100 46489101 G C 31 GENIC homozygous 637811551 6 46489719 46489720 C T 47 GENIC homozygous 637811552 6 46489750 46489751 C G 42 GENIC homozygous 637811553 6 46489800 46489801 A G 44 GENIC homozygous 637811554 6 46489815 46489816 C T 35 GENIC homozygous 637811555 6 46489905 46489906 G - 31 GENIC homozygous 749598706 6 46489926 46489927 C T 32 GENIC homozygous 637811556