chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51986190 51986191 A T 11 GENIC homozygous 114763826 13 51986806 51986807 C T 20 GENIC homozygous 114763832 13 51988597 51988598 G C 20 GENIC homozygous 114763834 13 51988797 51988798 C T 18 GENIC homozygous 114763836 13 51988816 51988817 C G 17 GENIC homozygous 114763838 13 51989893 51989894 T A 18 GENIC homozygous 114763840 13 51990048 51990049 C A 16 GENIC homozygous 114763842 13 51990250 51990251 A T 10 GENIC homozygous 114763844 13 51990255 51990256 G A 9 GENIC homozygous 114763846 13 51990500 51990501 T C 17 GENIC homozygous 114948529 13 51990501 51990502 G A 17 GENIC possibly homozygous 114948531 13 51992355 51992356 G A 6 GENIC homozygous 114763848