chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 205128834 205128835 G A 26 GENIC homozygous 562559338 4 205129264 205129265 A G 19 GENIC homozygous 562559339 4 205129586 205129587 T TG 20 GENIC homozygous 708249299 4 205129782 205129783 T C 17 GENIC homozygous 562559340 4 205129956 205129957 C T 25 GENIC possibly homozygous 562559341 4 205130242 205130243 C T 17 GENIC possibly homozygous 562559342 4 205130304 205130305 C T 11 GENIC possibly homozygous 562559343 4 205130305 205130306 T C 11 GENIC possibly homozygous 562559344 4 205130578 205130579 C T 6 GENIC heterozygous 562559345 4 205130927 205130928 C G 16 GENIC homozygous 562559346 4 205131056 205131057 T C 7 GENIC homozygous 562559347 4 205131067 205131068 A G 7 GENIC homozygous 562559348 4 205131439 205131440 G C 17 GENIC homozygous 562559349 4 205132645 205132646 G A 13 GENIC possibly homozygous 562559350 4 205133026 205133027 G A 7 GENIC possibly homozygous 565008107 4 205133039 205133040 A G 1 GENIC homozygous 562559351 4 205133447 205133448 G A 7 GENIC homozygous 562559352 4 205133966 205133967 C T 11 GENIC heterozygous 562559353 4 205134011 205134012 T C 7 GENIC homozygous 562559354 4 205134854 205134855 C T 25 GENIC possibly homozygous 562559355 4 205135577 205135578 C T 21 GENIC homozygous 562559356 4 205138221 205138222 T C 1 GENIC homozygous 562559357 4 205149823 205149824 T C 20 GENIC homozygous 562559358 4 205149920 205149921 T A 20 GENIC possibly homozygous 562559359