chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 40342687 40342689 CA -- 11 GENIC heterozygous 766168867 12 40349985 40349987 CA -- 12 GENIC heterozygous 766168868 12 40350572 40350573 T - 13 GENIC heterozygous 766168871 12 40350849 40350851 CA -- 6 GENIC heterozygous 766168873 12 40358199 40358200 T TC 26 GENIC homozygous 766168875 12 40358206 40358207 T TC 30 GENIC homozygous 766168876 12 40358210 40358211 G GC 30 GENIC homozygous 766168877 12 40358269 40358270 C CTG 8 GENIC heterozygous 766168880 12 40358280 40358282 TG -- 8 GENIC heterozygous 766168879 12 40358443 40358444 C G 12 GENIC homozygous 665011897 12 40358445 40358446 C G 12 GENIC homozygous 665011898 12 40363105 40363106 T - 9 GENIC heterozygous 766168881 12 40363888 40363889 A AGT 7 GENIC possibly homozygous 766168884 12 40364133 40364134 C CA 4 GENIC heterozygous 766168887