chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 2500795 2500796 C A 12 GENIC possibly homozygous 45076793 X 2505227 2505228 G A 23 GENIC homozygous 45076795 X 2508777 2508778 C T 20 GENIC homozygous 45076796 X 2510798 2510799 A - 15 GENIC possibly homozygous 45076799