chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 48289683 48289684 G A 38 GENIC homozygous 936097463 13 48290572 48290573 C T 29 GENIC homozygous 936097464 13 48291011 48291012 A G 29 GENIC homozygous 936097465 13 48291308 48291309 A T 30 GENIC homozygous 936097466 13 48291450 48291451 C T 14 GENIC homozygous 936097467 13 48291571 48291572 T C 21 GENIC homozygous 936097468 13 48292967 48292968 T C 32 GENIC homozygous 936097469 13 48294043 48294044 G A 20 GENIC homozygous 936097470 13 48296042 48296043 T A 24 GENIC homozygous 936097471 13 48296242 48296243 T C 21 GENIC homozygous 936097472 13 48296360 48296361 C G 8 GENIC homozygous 936097473 13 48296362 48296363 G T 7 GENIC homozygous 936097474 13 48296363 48296364 T A 7 GENIC homozygous 936097475 13 48296843 48296844 G A 34 GENIC homozygous 936097476 13 48296865 48296866 T A 35 GENIC homozygous 936097477 13 48296866 48296867 G T 35 GENIC homozygous 936097478 13 48297256 48297257 G T 23 GENIC homozygous 936097479 13 48297374 48297375 T C 24 GENIC homozygous 936097480