chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 12484573 12484574 G A 53 GENIC homozygous 503655470 17 12484759 12484760 A G 40 GENIC homozygous 503655471 17 12484846 12484847 C CCCA 27 GENIC homozygous 684800613 17 12484847 12484848 C CCA 29 GENIC homozygous 684800614 17 12485210 12485211 T C 53 GENIC possibly homozygous 503655472 17 12485304 12485306 GT -- 1 GENIC homozygous 684800615 17 12485467 12485468 T TCCC 2 GENIC homozygous 684800616 17 12485547 12485548 T C 30 GENIC homozygous 503655473 17 12486043 12486044 G A 59 GENIC homozygous 503655474 17 12486064 12486065 A G 55 GENIC homozygous 503655475 17 12486129 12486133 ACAT ---- 25 GENIC possibly homozygous 684800617 17 12486131 12486133 AT -- 29 GENIC possibly homozygous 684800618 17 12486136 12486144 CACATACC -------- 20 GENIC homozygous 684800619 17 12486151 12486157 CACGCA ------ 21 GENIC heterozygous 684800620 17 12486153 12486155 CG -- 21 GENIC possibly homozygous 684800621 17 12486179 12486182 CAC --- 34 GENIC heterozygous 684800622 17 12486181 12486182 C CA 33 GENIC heterozygous 684800623 17 12486186 12486187 C T 38 GENIC heterozygous 504091031 17 12486196 12486201 CCCAC ----- 28 GENIC heterozygous 684800624 17 12486205 12486206 T C 33 GENIC possibly homozygous 503655476 17 12486270 12486271 C T 45 GENIC homozygous 503655477 17 12486324 12486325 G A 60 GENIC homozygous 503655478 17 12486969 12486970 T C 42 GENIC homozygous 503655479 17 12487518 12487519 G A 38 GENIC homozygous 504091032 17 12488656 12488657 C G 36 GENIC possibly homozygous 503655480 17 12490401 12490402 G T 36 GENIC possibly homozygous 504091033 17 12490480 12490481 C T 25 GENIC possibly homozygous 503655481 17 12490526 12490527 T G 19 GENIC homozygous 503655482 17 12490535 12490536 A G 20 GENIC homozygous 503655483