chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 51050599 51050600 A ACG 23 INTERGENIC homozygous 49755760 13 51053147 51053148 T - 24 INTERGENIC homozygous 49755765 13 51058895 51058896 A ATG 9 INTERGENIC heterozygous 49755766 13 51058895 51058896 A ATGTG 9 INTERGENIC heterozygous 49755767 13 51059829 51059833 AAGA ---- 6 INTERGENIC homozygous 50617180 13 51067416 51067420 CTTT ---- 10 INTERGENIC homozygous 50550975 13 51067560 51067572 TTCTTTCTTTCT ------------ 24 INTERGENIC homozygous 50562999 13 51072225 51072226 G - 32 INTERGENIC homozygous 49755769 13 51072243 51072244 C - 23 INTERGENIC homozygous 49755770 13 51072254 51072255 C A 22 INTERGENIC homozygous 49755771 13 51072267 51072268 A G 23 INTERGENIC homozygous 49755772 13 51072283 51072284 A T 26 INTERGENIC homozygous 49755773 13 51072408 51072409 A T 36 INTERGENIC homozygous 49755774 13 51072416 51072417 C CA 35 INTERGENIC homozygous 49755775 13 51072443 51072444 T TA 24 INTERGENIC homozygous 49755776 13 51072449 51072450 T C 28 INTERGENIC homozygous 49755777 13 51072457 51072458 G GA 26 INTERGENIC homozygous 49755778 13 51072464 51072465 T TA 26 INTERGENIC homozygous 49755779 13 51072469 51072470 A C 29 INTERGENIC homozygous 49755780 13 51075007 51075008 G C 28 INTERGENIC homozygous 49755781 13 51075033 51075034 A C 37 INTERGENIC homozygous 49755782 13 51075648 51075649 T C 32 INTERGENIC homozygous 49755783 13 51076068 51076069 G GCA 16 INTERGENIC homozygous 49755784 13 51075683 51075684 T G 29 INTERGENIC homozygous 49947064 13 51075684 51075685 G T 29 INTERGENIC homozygous 49947065 13 51075649 51075650 C A 32 INTERGENIC homozygous 50495113