chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 75199261 75199262 G A 11 GENIC homozygous 50095791 13 75199725 75199726 C T 16 GENIC homozygous 50095793 13 75200065 75200066 G A 20 GENIC homozygous 50095795 13 75200423 75200424 G T 10 GENIC homozygous 50095797 13 75200438 75200440 GG -- 8 GENIC homozygous 50095799 13 75200448 75200449 G C 8 GENIC homozygous 51266904 13 75203375 75203376 G GATT 8 GENIC homozygous 49818896 13 75204410 75204411 C CTCCTT 13 GENIC homozygous 50095809 13 75204524 75204525 T C 13 GENIC homozygous 50095813 13 75204677 75204678 T C 12 GENIC homozygous 49818897 13 75205884 75205885 A G 8 GENIC homozygous 50095815 13 75206266 75206267 C T 14 GENIC homozygous 50095817 13 75206644 75206645 A G 11 GENIC homozygous 50095819 13 75207010 75207022 CAGGGCTGCGGG ------------ 13 GENIC homozygous 50095821 13 75207483 75207484 A G 17 GENIC homozygous 49818900 13 75210453 75210456 TAA --- 12 GENIC homozygous 49818903 13 75211437 75211438 C G 13 GENIC homozygous 49818904 13 75212432 75212433 G A 11 GENIC homozygous 50095825 13 75216316 75216317 G GT 7 GENIC homozygous 50095827 13 75216628 75216629 T C 15 GENIC homozygous 49818906 13 75216789 75216790 T C 12 GENIC homozygous 49818907 13 75217047 75217048 A G 8 GENIC homozygous 49818908 13 75217098 75217099 A C 11 GENIC homozygous 49818909 13 75217099 75217100 G T 11 GENIC homozygous 49818910 13 75218446 75218447 A AG 7 GENIC homozygous 50095829 13 75220559 75220560 A G 17 GENIC homozygous 49818916 13 75222735 75222736 T C 12 GENIC homozygous 49818919 13 75223821 75223822 C A 12 GENIC homozygous 49818921 13 75224111 75224112 C T 17 GENIC homozygous 49818922 13 75225581 75225582 A G 21 GENIC homozygous 49818923 13 75226753 75226754 G T 14 GENIC homozygous 49818929 13 75229462 75229463 G A 15 GENIC homozygous 50095837