chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 15833674 15833675 T - 5 GENIC homozygous 45097651 X 15833897 15833898 A ATT 10 GENIC heterozygous 45097652 X 15833897 15833898 A AT 10 GENIC heterozygous 45473857 X 15835272 15835273 G GT 11 GENIC homozygous 45273989 X 15835350 15835351 T - 9 GENIC possibly homozygous 45473859 X 15835953 15835954 A ATTTGTTTG 8 GENIC homozygous 45097655 X 15836449 15836450 G GCA 1 GENIC homozygous 45273990 X 15836461 15836462 G GCACGCACACACACACA 3 GENIC heterozygous 45501241 X 15836617 15836618 C T 8 GENIC homozygous 45273991 X 15836829 15836830 A G 11 GENIC homozygous 45273992 X 15837186 15837187 A AAAGGAGG 16 GENIC homozygous 45473861 X 15837189 15837190 C A 16 GENIC homozygous 45473863 X 15837190 15837191 T TGAAAAGAAA 15 GENIC homozygous 45273994 X 15837192 15837193 C A 15 GENIC homozygous 45795328 X 15837195 15837196 G GAGGA 15 GENIC homozygous 45273995 X 15838201 15838210 ATGCTTATA --------- 6 GENIC homozygous 45097658 X 15838325 15838329 CCCT ---- 2 GENIC homozygous 45795329