chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 62799094 62799095 T C 33 GENIC homozygous 116837761 8 62799494 62799495 A G 23 GENIC homozygous 116837765 8 62800171 62800172 A G 25 GENIC homozygous 116837773 8 62801077 62801078 G A 18 GENIC homozygous 116837777 8 62801160 62801161 A G 11 GENIC homozygous 116837779 8 62801586 62801587 G T 13 GENIC homozygous 116837781 8 62802134 62802135 C T 7 GENIC homozygous 116837783 8 62803088 62803089 G A 20 GENIC homozygous 117143229 8 62803358 62803359 A G 20 GENIC homozygous 116837785 8 62804886 62804887 C T 27 GENIC homozygous 117143233 8 62805112 62805115 TCC 16 GENIC homozygous 130363632 8 62799397 62799398 T 21 GENIC homozygous 130363627 8 62800298 62800299 T 24 GENIC homozygous 130363628 8 62800342 62800344 AC 13 GENIC homozygous 130363629 8 62800373 62800373 T 9 GENIC homozygous 130363630 8 62804140 62804140 A 6 GENIC heterozygous 130363631 8 62805119 62805121 AC 16 GENIC homozygous 130363633 8 62805122 62805122 AGGAGAG 16 GENIC homozygous 130363634 8 62805354 62805355 C T 18 GENIC homozygous 130372651 8 62809068 62809069 A G 11 GENIC homozygous 116837791 8 62807445 62807445 TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT 12 GENIC heterozygous 131693726