chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 28450830 28450831 T C 14 GENIC homozygous 801267350 X 28459909 28459910 C T 16 GENIC homozygous 801267351 X 28460127 28460128 G T 9 GENIC homozygous 801267352 X 28460532 28460533 G A 9 GENIC homozygous 801267353 X 28461085 28461086 A G 19 GENIC homozygous 801267354 X 28462942 28462943 G A 7 GENIC homozygous 801267355 X 28463517 28463518 C T 17 GENIC homozygous 801267356 X 28464376 28464377 C T 3 GENIC homozygous 801267357 X 28464534 28464535 G A 13 GENIC heterozygous 801267358 X 28465225 28465226 T C 23 GENIC possibly homozygous 801267359 X 28465560 28465561 A G 13 GENIC homozygous 801267360 X 28465565 28465566 A G 12 GENIC homozygous 801267361 X 28468275 28468276 A C 11 GENIC heterozygous 801267362 X 28468279 28468280 A C 10 GENIC heterozygous 801267363 X 28468283 28468284 A C 9 GENIC heterozygous 801267364 X 28468287 28468288 A C 10 GENIC heterozygous 801267365 X 28468321 28468322 T G 6 GENIC heterozygous 801267366