chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 52664851 52664852 T G 21 GENIC homozygous 114550692 13 52666742 52666743 T A 25 GENIC homozygous 114550693 13 52667915 52667916 T C 17 GENIC homozygous 114550694 13 52667921 52667922 C T 17 GENIC homozygous 114550695 13 52668677 52668678 A G 47 GENIC homozygous 114550696 13 52668753 52668754 C T 43 GENIC homozygous 114550697 13 52668920 52668921 A G 27 GENIC homozygous 114550698 13 52671635 52671636 A G 13 GENIC homozygous 114967755 13 52673254 52673255 G A 13 GENIC homozygous 114617568 13 52673586 52673587 T C 26 GENIC homozygous 114550699 13 52674966 52674967 C T 26 GENIC homozygous 114550700 13 52675188 52675189 G A 39 GENIC homozygous 114550701 13 52675893 52675894 A C 20 GENIC homozygous 114550702 13 52677654 52677655 C T 37 GENIC homozygous 114550703 13 52679629 52679630 T C 20 GENIC homozygous 114550704 13 52680009 52680010 G A 20 GENIC homozygous 114550705