chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 62046004 62046005 A G 15 GENIC homozygous 46486130 18 62047236 62047237 A G 22 GENIC homozygous 46486132 18 62047981 62047983 TT -- 17 GENIC possibly homozygous 46486133 18 62047982 62047983 T - 17 GENIC heterozygous 46486135 18 62049487 62049488 A - 34 GENIC homozygous 46486137 18 62050323 62050324 A G 17 GENIC homozygous 46486139 18 62051225 62051226 G GAGGAGAAGGAGA 10 GENIC homozygous 46898531 18 62052045 62052047 GT -- 13 GENIC homozygous 46486147 18 62052226 62052227 C T 17 GENIC homozygous 46486149 18 62053943 62053944 C CTAGA 16 GENIC homozygous 46880071 18 62057379 62057380 G C 34 GENIC homozygous 46486151 18 62057844 62057845 G A 28 GENIC homozygous 46486153 18 62058785 62058786 C CTTT 18 GENIC possibly homozygous 46486154 18 62058785 62058786 C CT 18 GENIC heterozygous 46613787 18 62058785 62058786 C CTT 18 GENIC heterozygous 46613788 18 62060545 62060546 A G 14 GENIC homozygous 46486156 18 62060875 62060876 G A 20 GENIC homozygous 46486158 18 62061272 62061273 T C 12 GENIC homozygous 46486160 18 62061366 62061367 C CT 11 GENIC possibly homozygous 46486162 18 62061437 62061438 C CAAAT 8 GENIC homozygous 46486163