chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 62279071 62279072 A G 16 GENIC homozygous 939677159 18 62279284 62279285 C T 22 GENIC homozygous 939677160 18 62279394 62279395 A G 19 GENIC homozygous 939677161 18 62279435 62279436 C T 23 GENIC homozygous 939677162 18 62279446 62279447 C T 21 GENIC homozygous 939677163 18 62279544 62279545 T C 11 GENIC homozygous 939677164 18 62279676 62279677 T C 19 GENIC homozygous 939677165 18 62279715 62279716 T C 11 GENIC homozygous 939677166 18 62280553 62280554 T A 15 GENIC homozygous 939677167 18 62280603 62280604 C T 11 GENIC homozygous 939677168 18 62280890 62280891 T C 19 GENIC homozygous 939677169 18 62281059 62281060 G C 19 GENIC homozygous 939677170 18 62281334 62281335 C T 23 GENIC homozygous 939677171 18 62281608 62281609 A T 28 GENIC homozygous 939677172 18 62287111 62287112 T A 15 GENIC homozygous 939677173 18 62287274 62287275 A G 20 GENIC homozygous 939677174 18 62287300 62287301 T C 21 GENIC homozygous 939677175 18 62287356 62287357 C T 22 GENIC homozygous 939677176