chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 41722157 41722158 C CGTGTGT 8 GENIC possibly homozygous 766564761 17 41724689 41724690 C T 27 GENIC homozygous 665691815 17 41725524 41725525 C T 33 GENIC homozygous 665691816 17 41725638 41725639 G T 22 GENIC homozygous 665691817 17 41726213 41726215 AG -- 9 GENIC homozygous 766564762 17 41726722 41726723 T C 36 GENIC homozygous 665691818 17 41730111 41730112 G GATAT 39 GENIC homozygous 766564763 17 41730112 41730113 C CTCTAGA 39 GENIC homozygous 766564764 17 41730719 41730720 G T 19 GENIC homozygous 665691819 17 41730794 41730795 T C 19 GENIC homozygous 665691820