chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 17344191 17344192 G T 16 GENIC homozygous 115365079 12 17344392 17344393 A G 25 GENIC homozygous 115365080 12 17344670 17344671 T C 23 GENIC homozygous 115365081 12 17344807 17344808 T C 9 GENIC homozygous 115365082 12 17345142 17345143 T C 17 GENIC homozygous 115365083 12 17345985 17345986 C T 20 GENIC homozygous 115365084 12 17346189 17346190 A G 25 GENIC homozygous 115365085 12 17346271 17346272 T C 14 GENIC homozygous 115421341 12 17346364 17346365 T C 24 GENIC homozygous 115273561 12 17347062 17347063 A G 21 GENIC homozygous 115273563 12 17348831 17348832 A G 13 GENIC homozygous 115365086 12 17349307 17349308 T C 16 GENIC homozygous 115273565 12 17350951 17350952 G A 25 GENIC homozygous 115365087 12 17351964 17351965 T C 24 GENIC homozygous 115365088 12 17353329 17353330 A G 26 GENIC homozygous 115273573 12 17354336 17354337 A T 24 GENIC homozygous 115273575 12 17354338 17354339 T G 25 GENIC homozygous 115273576 12 17354515 17354516 A G 22 GENIC homozygous 115273580 12 17356326 17356327 C T 30 GENIC homozygous 115273584 12 17357171 17357172 G A 24 GENIC homozygous 115365089 12 17357452 17357453 G C 15 GENIC homozygous 115273586 12 17357535 17357536 T C 17 GENIC homozygous 115273588