chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 89602165 89602166 A G 27 INTERGENIC homozygous 49856268 13 89602693 89602694 A G 17 INTERGENIC homozygous 49856269 13 89602711 89602712 A C 19 INTERGENIC homozygous 49856270 13 89602869 89602870 A C 19 INTERGENIC homozygous 49856271 13 89603181 89603182 G A 24 INTERGENIC homozygous 49856272 13 89603686 89603687 A G 19 INTERGENIC homozygous 49856273 13 89603688 89603689 G A 19 INTERGENIC homozygous 49856274 13 89603712 89603713 G A 19 INTERGENIC homozygous 49856275 13 89603715 89603716 T G 19 INTERGENIC homozygous 49856276 13 89603716 89603717 A C 20 INTERGENIC homozygous 49856277 13 89603850 89603851 C T 15 INTERGENIC homozygous 49856278 13 89603929 89603930 A - 12 INTERGENIC homozygous 49856279 13 89604023 89604024 C T 15 INTERGENIC homozygous 49856280 13 89604052 89604053 C G 10 INTERGENIC homozygous 49856281 13 89604560 89604561 C T 27 INTERGENIC homozygous 49856290 13 89604679 89604680 A G 29 INTERGENIC homozygous 49856293 13 89605445 89605446 T TCA 28 INTERGENIC homozygous 49856294 13 89605625 89605626 G A 34 INTERGENIC homozygous 49856295 13 89605745 89605746 T C 23 INTERGENIC homozygous 49856296 13 89605831 89605832 G A 22 INTERGENIC homozygous 49856297 13 89606051 89606052 G C 27 INTERGENIC homozygous 49856299