chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 100296227 100296228 C CT 7 GENIC heterozygous 48719871 15 100296227 100296228 C CTT 7 GENIC heterozygous 48531175 15 100297252 100297253 G C 11 GENIC homozygous 48402972 15 100296718 100296719 C G 26 GENIC homozygous 48402969 15 100297240 100297241 T C 12 GENIC homozygous 48402970 15 100297249 100297250 G C 12 GENIC homozygous 48402971 15 100297256 100297257 G C 10 GENIC homozygous 48402973 15 100297265 100297266 T C 9 GENIC homozygous 48402974 15 100297270 100297271 T C 8 GENIC homozygous 48402975 15 100297279 100297280 T C 5 GENIC homozygous 48402976 15 100297290 100297291 T C 5 GENIC homozygous 48402977 15 100297293 100297294 T C 5 GENIC homozygous 48402978 15 100297298 100297299 A AG 5 GENIC homozygous 48402979 15 100297301 100297302 T TTC 5 GENIC homozygous 48402980 15 100297306 100297307 T TC 2 GENIC homozygous 48402981 15 100297681 100297682 T G 19 GENIC homozygous 48402982 15 100297684 100297685 G GC 18 GENIC homozygous 48531177 15 100297787 100297790 TTC --- 10 GENIC homozygous 48531179 15 100297826 100297827 T - 10 GENIC homozygous 48531181 15 100297860 100297861 A AC 18 GENIC homozygous 48531183 15 100298522 100298523 T G 24 GENIC homozygous 48531185 15 100298856 100298857 G A 13 GENIC homozygous 48531187 15 100299585 100299586 T G 17 GENIC homozygous 48531189 15 100302694 100302695 T C 41 GENIC homozygous 48402988