chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89991015 89991016 G T 34 INTERGENIC homozygous 944959033 13 89991053 89991054 T A 33 INTERGENIC homozygous 944959034 13 89991068 89991069 T C 29 INTERGENIC homozygous 944959035 13 89991113 89991114 G A 27 INTERGENIC homozygous 944959036 13 89991141 89991142 T C 29 INTERGENIC homozygous 944959037 13 89991239 89991240 G T 37 INTERGENIC homozygous 944959038 13 89991414 89991415 C T 29 INTERGENIC homozygous 944959039 13 89992204 89992205 G C 31 INTERGENIC homozygous 944959040 13 89992207 89992208 C T 37 INTERGENIC homozygous 944959041 13 89992238 89992239 C T 39 INTERGENIC homozygous 944959042 13 89992610 89992611 C T 35 INTERGENIC homozygous 944959043 13 89993796 89993797 A G 36 INTERGENIC homozygous 944959044 13 89993978 89993979 T G 31 INTERGENIC homozygous 944959045 13 89994724 89994725 C G 35 INTERGENIC homozygous 944959046 13 89994932 89994933 G A 34 INTERGENIC homozygous 944959047 13 89995140 89995141 G C 20 INTERGENIC homozygous 944959048 13 89995166 89995167 C T 29 INTERGENIC homozygous 944959049 13 89995203 89995204 G A 35 INTERGENIC homozygous 944959050 13 89995407 89995408 G T 22 INTERGENIC homozygous 944959051 13 89995825 89995826 T G 33 INTERGENIC homozygous 944959052 13 89995849 89995850 C T 24 INTERGENIC homozygous 944959053 13 89995966 89995967 A G 27 INTERGENIC homozygous 944959054