chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 95208775 95208776 C - 34 GENIC homozygous 761866212 13 95209885 95209886 A AC 93 GENIC homozygous 761866213 13 95209891 95209894 CAA --- 97 GENIC homozygous 761866214 13 95209908 95209910 CA -- 56 GENIC heterozygous 761866215 13 95211420 95211421 C CTG 8 GENIC heterozygous 761866219 13 95215416 95215417 C CTGTG 12 GENIC homozygous 761866224 13 95216891 95216892 A C 37 GENIC homozygous 657990822 13 95216893 95216894 T - 37 GENIC homozygous 761866225 13 95216898 95216899 C - 38 GENIC homozygous 761866226 13 95216907 95216908 A - 40 GENIC homozygous 761866227 13 95216909 95216910 T C 38 GENIC homozygous 657990823