chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 70626016 70626017 T C 11 GENIC homozygous 113349581 4 70626079 70626080 T C 11 GENIC homozygous 113032317 4 70626506 70626507 A G 21 GENIC homozygous 113032320 4 70626677 70626678 T C 13 GENIC homozygous 113032321 4 70626851 70626852 C T 29 GENIC homozygous 113032322 4 70627071 70627072 C A 14 GENIC homozygous 113032326 4 70627074 70627075 T C 14 GENIC homozygous 113032327 4 70627361 70627362 G T 27 GENIC possibly homozygous 113032328 4 70627428 70627429 A T 21 GENIC homozygous 113032329 4 70627533 70627534 A G 21 GENIC homozygous 113032330 4 70627717 70627718 G T 20 GENIC homozygous 113349583 4 70627742 70627743 C T 16 GENIC homozygous 113032331 4 70627774 70627775 T G 10 GENIC homozygous 113349585 4 70627797 70627798 A T 9 GENIC homozygous 113032332 4 70627842 70627843 G T 19 GENIC homozygous 113032334 4 70627894 70627895 A T 19 GENIC homozygous 113032335 4 70627903 70627904 G T 15 GENIC homozygous 113032336 4 70627953 70627954 G A 8 GENIC homozygous 113032337 4 70628088 70628089 G A 12 GENIC homozygous 113032338 4 70628103 70628104 A G 14 GENIC homozygous 113032339 4 70628120 70628121 T C 15 GENIC homozygous 113032340 4 70628195 70628196 C T 14 GENIC homozygous 113032341 4 70628234 70628235 C T 17 GENIC homozygous 113032342 4 70628281 70628282 G C 15 GENIC homozygous 113032343 4 70628319 70628320 G A 16 GENIC homozygous 113032344 4 70628445 70628446 T A 30 GENIC homozygous 113032345 4 70626442 70626443 A C 30 GENIC heterozygous 113512226 4 70626455 70626456 C A 29 GENIC heterozygous 113594085 4 70626457 70626458 G A 27 GENIC heterozygous 113594087