chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 90559769 90559770 C A 11 INTERGENIC heterozygous 52396586 10 90559862 90559863 C T 8 INTERGENIC possibly homozygous 52396588 10 90560123 90560124 G T 22 INTERGENIC homozygous 51736984 10 90560357 90560360 CCC --- 2 INTERGENIC heterozygous 52396590 10 90560814 90560815 C T 16 INTERGENIC possibly homozygous 52396592 10 90560833 90560834 C T 11 INTERGENIC heterozygous 52396594 10 90560928 90560929 C T 27 INTERGENIC possibly homozygous 52206568 10 90561642 90561643 G GAC 9 INTERGENIC homozygous 52396602 10 90562239 90562240 G T 13 INTERGENIC homozygous 51737002 10 90562345 90562346 A AT 1 INTERGENIC homozygous 52396604 10 90562481 90562482 G T 3 INTERGENIC homozygous 51737004 10 90564617 90564618 A C 10 INTERGENIC homozygous 52206580 10 90564647 90564648 C T 15 INTERGENIC possibly homozygous 51737012 10 90564681 90564682 A G 11 INTERGENIC heterozygous 51737014 10 90564747 90564748 T C 12 INTERGENIC homozygous 51737016 10 90565103 90565104 C T 13 INTERGENIC homozygous 52323212 10 90565105 90565106 T C 13 INTERGENIC homozygous 52323214 10 90565116 90565117 A G 7 INTERGENIC homozygous 51737019 10 90565125 90565129 GCTG ---- 6 INTERGENIC homozygous 51737021 10 90565198 90565199 G A 20 INTERGENIC possibly homozygous 51737023 10 90565243 90565244 T C 27 INTERGENIC homozygous 51737025 10 90565277 90565278 C T 22 INTERGENIC possibly homozygous 51737027 10 90565426 90565427 A T 24 INTERGENIC possibly homozygous 51737031 10 90565475 90565476 C T 13 INTERGENIC homozygous 51737032 10 90565869 90565870 G A 17 INTERGENIC possibly homozygous 51737034