chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89602165 89602166 A G 28 INTERGENIC possibly homozygous 49856268 13 89602693 89602694 A G 22 INTERGENIC homozygous 49856269 13 89602711 89602712 A C 23 INTERGENIC homozygous 49856270 13 89602869 89602870 A C 32 INTERGENIC homozygous 49856271 13 89603181 89603182 G A 20 INTERGENIC homozygous 49856272 13 89603686 89603687 A G 12 INTERGENIC homozygous 49856273 13 89603688 89603689 G A 12 INTERGENIC homozygous 49856274 13 89603712 89603713 G A 9 INTERGENIC homozygous 49856275 13 89603715 89603716 T G 9 INTERGENIC homozygous 49856276 13 89603716 89603717 A C 9 INTERGENIC homozygous 49856277 13 89603850 89603851 C T 14 INTERGENIC possibly homozygous 49856278 13 89603929 89603930 A - 17 INTERGENIC possibly homozygous 49856279 13 89604023 89604024 C T 13 INTERGENIC homozygous 49856280 13 89604052 89604053 C G 12 INTERGENIC homozygous 49856281 13 89604560 89604561 C T 35 INTERGENIC homozygous 49856290 13 89604679 89604680 A G 37 INTERGENIC homozygous 49856293 13 89605445 89605446 T TCA 43 INTERGENIC homozygous 49856294 13 89605625 89605626 G A 28 INTERGENIC homozygous 49856295 13 89605745 89605746 T C 34 INTERGENIC possibly homozygous 49856296 13 89605831 89605832 G A 16 INTERGENIC homozygous 49856297 13 89606051 89606052 G C 35 INTERGENIC homozygous 49856299