chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 9552033 9552034 C T 14 GENIC homozygous 805077302 17 9552155 9552156 T C 24 GENIC homozygous 805077303 17 9553146 9553147 A G 30 GENIC homozygous 805077304 17 9553389 9553390 T C 22 GENIC homozygous 805077305 17 9553939 9553940 G A 33 GENIC heterozygous 805077306 17 9553948 9553949 G A 32 GENIC heterozygous 805077307 17 9553960 9553961 A G 28 GENIC heterozygous 805077308 17 9553976 9553977 G A 22 GENIC heterozygous 805077309 17 9554075 9554076 T G 15 GENIC homozygous 805077310 17 9554866 9554867 G A 33 GENIC homozygous 805077311 17 9555004 9555005 G T 23 GENIC homozygous 805077312 17 9555084 9555085 T A 19 GENIC homozygous 805077313 17 9556236 9556237 A G 29 GENIC homozygous 805077314 17 9556553 9556554 C T 23 GENIC homozygous 805077315 17 9557398 9557399 G A 14 GENIC homozygous 805077316 17 9557437 9557438 C A 12 GENIC homozygous 805077317 17 9557955 9557956 G A 31 GENIC possibly homozygous 805077318 17 9558576 9558577 T C 34 GENIC homozygous 805077319