chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 95463020 95463021 G A 12 GENIC homozygous 823837398 13 95463809 95463810 T C 10 GENIC homozygous 823837399 13 95464098 95464099 C G 7 GENIC homozygous 823837400 13 95464247 95464248 G - 8 GENIC homozygous 823837401 13 95464273 95464274 G GT 10 GENIC homozygous 823837402 13 95464277 95464278 G - 10 GENIC homozygous 823837403 13 95464543 95464544 A G 9 GENIC homozygous 823837404 13 95464891 95464892 T C 8 GENIC homozygous 823837405 13 95465177 95465178 A G 9 GENIC homozygous 823837406 13 95467123 95467124 C T 10 GENIC homozygous 823837407 13 95467304 95467305 G T 15 GENIC homozygous 823837408 13 95468223 95468224 T C 17 GENIC homozygous 823837409 13 95468753 95468754 T A 12 GENIC homozygous 823837410 13 95468824 95468825 T G 11 GENIC homozygous 823837411 13 95468925 95468926 G A 15 GENIC homozygous 823837412