chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 105048691 105048692 C G 12 GENIC homozygous 113694002 14 105048871 105048872 C G 17 GENIC homozygous 113615836 14 105049501 105049502 G A 26 GENIC homozygous 113615837 14 105049511 105049512 T C 27 GENIC homozygous 113615838 14 105050360 105050361 G A 20 GENIC homozygous 113615839 14 105051964 105051965 G A 18 GENIC homozygous 113532045 14 105052745 105052746 A G 31 GENIC homozygous 113615840 14 105052890 105052891 C T 27 GENIC homozygous 113615841 14 105053025 105053026 G C 39 GENIC homozygous 113615842 14 105053304 105053305 C T 34 GENIC heterozygous 114224376 14 105054382 105054383 A G 25 GENIC homozygous 113615843 14 105053342 105053343 C A 26 GENIC heterozygous 113764745