chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 48288391 48288392 C G 49 GENIC homozygous 809053188 13 48289539 48289540 A G 58 GENIC homozygous 809053189 13 48289683 48289684 G A 55 GENIC homozygous 809053190 13 48290461 48290462 C T 47 GENIC homozygous 809053191 13 48290478 48290479 T A 45 GENIC homozygous 809053192 13 48290648 48290649 G A 45 GENIC homozygous 809053193 13 48290827 48290828 G A 49 GENIC homozygous 809053194 13 48291011 48291012 A G 47 GENIC homozygous 809053195 13 48291308 48291309 A T 52 GENIC homozygous 809053196 13 48291571 48291572 T C 62 GENIC possibly homozygous 809053197 13 48292967 48292968 T C 54 GENIC homozygous 809053198 13 48294489 48294490 T A 35 GENIC homozygous 809053199 13 48295197 48295198 G A 35 GENIC heterozygous 809053200 13 48296042 48296043 T A 34 GENIC homozygous 809053201 13 48296242 48296243 T C 21 GENIC homozygous 809053202 13 48296271 48296272 G A 14 GENIC homozygous 809053203 13 48296328 48296329 G T 37 GENIC homozygous 809053204 13 48296341 48296342 A G 14 GENIC homozygous 809053205 13 48296843 48296844 G A 44 GENIC homozygous 809053206 13 48296866 48296867 G T 27 GENIC homozygous 809053207 13 48297374 48297375 T C 53 GENIC homozygous 809053208