chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 41739933 41739934 A G 31 GENIC homozygous 114541096 13 41740554 41740555 T C 31 GENIC homozygous 114329878 13 41741000 41741001 T C 24 GENIC homozygous 114329880 13 41742308 41742309 G A 10 GENIC homozygous 114329882 13 41743203 41743204 A G 29 GENIC homozygous 114329884 13 41743594 41743595 C T 25 GENIC homozygous 114329886 13 41747233 41747234 C T 34 GENIC homozygous 114329888 13 41747305 41747306 T C 27 GENIC homozygous 114329890 13 41747761 41747762 C T 32 GENIC homozygous 114329892 13 41748428 41748429 C A 29 GENIC homozygous 114329894 13 41749680 41749681 G A 28 GENIC homozygous 114329896 13 41750028 41750029 T C 16 GENIC homozygous 114329898 13 41750209 41750224 CTGACTAATTCAGTA 20 GENIC homozygous 129046427 13 41743198 41743200 TA 29 GENIC homozygous 129046425 13 41743448 41743449 C T 27 GENIC homozygous 114821365 13 41749887 41749888 C T 18 GENIC homozygous 114821367 13 41744742 41744743 C G 4 GENIC homozygous 129108544 13 41744744 41744745 C G 4 GENIC homozygous 129108545 13 41744746 41744747 C G 4 GENIC homozygous 129108546 13 41751906 41751907 A C 28 GENIC homozygous 114329900 13 41752354 41752355 G T 31 GENIC homozygous 114329902 13 41753169 41753169 G 17 GENIC homozygous 129046428 13 41755237 41755237 A 27 GENIC homozygous 129046429 13 41755431 41755432 T A 23 GENIC homozygous 114329904 13 41758730 41758731 C T 20 GENIC possibly homozygous 114329906 13 41758850 41758851 G A 30 GENIC homozygous 114329908 13 41758911 41758912 G C 27 GENIC homozygous 114329910