chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 13091642 13091643 A G 22 GENIC homozygous 115259742 12 13092512 13092513 G A 18 GENIC homozygous 115259746 12 13093250 13093251 G A 41 GENIC homozygous 115416641 12 13096700 13096701 G A 28 GENIC homozygous 115259750 12 13098210 13098211 G C 27 GENIC homozygous 115259752 12 13098484 13098485 A C 18 GENIC homozygous 115416643 12 13102473 13102474 T C 22 GENIC homozygous 115259756 12 13103676 13103677 C T 26 GENIC homozygous 115259758 12 13103844 13103845 A T 21 GENIC possibly homozygous 115259760 12 13104281 13104282 G A 37 GENIC homozygous 115259762 12 13105348 13105349 C T 27 GENIC homozygous 115416645 12 13107182 13107183 C T 19 GENIC homozygous 115259768 12 13109211 13109212 C T 27 GENIC homozygous 115259772 12 13109316 13109317 G A 31 GENIC homozygous 115259774 12 13110695 13110696 T C 24 GENIC homozygous 115259776 12 13111748 13111749 A G 33 GENIC homozygous 115416647