chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 79696845 79696846 T G 16 GENIC possibly homozygous 50106988 13 79697213 79697214 G A 17 GENIC possibly homozygous 50106990 13 79697405 79697406 A G 13 GENIC homozygous 50106992 13 79703698 79703699 T C 25 GENIC possibly homozygous 50106996 13 79704852 79704853 C A 20 GENIC homozygous 50106998 13 79707153 79707154 C T 14 GENIC possibly homozygous 50107000 13 79707195 79707196 C CATGGTGT 2 GENIC homozygous 50107002 13 79707377 79707378 A - 11 GENIC homozygous 50107004 13 79707721 79707722 G T 9 GENIC homozygous 49832463 13 79707723 79707727 TAAC ---- 9 GENIC homozygous 49832464 13 79708233 79708237 AACC ---- 4 GENIC homozygous 50107006 13 79708422 79708423 C T 5 GENIC heterozygous 50107008 13 79708423 79708424 A G 5 GENIC heterozygous 50107010 13 79708468 79708469 C A 4 GENIC homozygous 50107012 13 79708478 79708479 A C 5 GENIC homozygous 50107014 13 79708581 79708582 A G 18 GENIC homozygous 50107016 13 79709884 79709885 A - 14 GENIC possibly homozygous 50107018 13 79709978 79709979 A G 14 GENIC homozygous 50107020 13 79710143 79710144 A G 13 GENIC homozygous 50107022 13 79711303 79711304 C G 7 GENIC possibly homozygous 49832466 13 79712213 79712214 A G 11 GENIC heterozygous 50107030 13 79710667 79710668 T C 16 GENIC possibly homozygous 50107024 13 79710863 79710864 A G 6 GENIC homozygous 50107026 13 79712936 79712937 T C 9 GENIC homozygous 50107032 13 79714402 79714403 C T 12 GENIC homozygous 50107034 13 79714942 79714943 G A 19 GENIC possibly homozygous 50107036 13 79716646 79716647 C - 5 GENIC homozygous 49832468 13 79714977 79714978 T C 21 GENIC homozygous 50107038 13 79716282 79716283 C A 11 GENIC homozygous 50107044