chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 51336866 51336867 T C 30 GENIC homozygous 61868001 1 51337110 51337111 A G 35 GENIC homozygous 61868002 1 51337379 51337380 T TCC 30 GENIC homozygous 61868003 1 51337380 51337381 A T 31 GENIC homozygous 62127211 1 51337521 51337522 T A 32 GENIC homozygous 61868004 1 51337713 51337714 C CCACACACACACA 11 GENIC heterozygous 62127212 1 51337713 51337714 C CCACACACACACACA 11 GENIC heterozygous 62127213 1 51337774 51337775 A AT 19 GENIC homozygous 61868007 1 51337829 51337830 T C 22 GENIC homozygous 61868008 1 51337964 51337965 C T 23 GENIC homozygous 61868009 1 51338329 51338330 G A 23 GENIC homozygous 61868010 1 51338450 51338451 C T 25 GENIC homozygous 61868011 1 51338512 51338513 T C 30 GENIC homozygous 61868012 1 51338588 51338589 T C 25 GENIC homozygous 61868013 1 51338726 51338727 C T 40 GENIC homozygous 61868014 1 51338733 51338734 T C 39 GENIC homozygous 61868015 1 51339854 51339855 C T 30 GENIC homozygous 61868016 1 51339999 51340000 C T 36 GENIC homozygous 61868017 1 51340482 51340483 C T 34 GENIC homozygous 61868018 1 51340703 51340704 A - 19 GENIC possibly homozygous 61412936 1 51341133 51341134 A G 24 GENIC homozygous 61868019