chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 90211441 90211442 G A 26 GENIC homozygous 68165194 10 90212356 90212357 G A 25 GENIC homozygous 68165197 10 90214177 90214178 C T 28 GENIC homozygous 68455203 10 90214912 90214913 T A 28 GENIC homozygous 68165200 10 90215154 90215155 G A 23 GENIC homozygous 68165203 10 90216961 90216962 T C 35 GENIC homozygous 68165206 10 90219945 90219946 C A 18 GENIC homozygous 68165219 10 90219951 90219952 C A 16 GENIC homozygous 68165222 10 90220311 90220312 G A 34 GENIC possibly homozygous 68165225 10 90221554 90221555 A C 19 GENIC possibly homozygous 68165228 10 90221782 90221783 A G 20 GENIC homozygous 68165231 10 90222434 90222435 T C 29 GENIC homozygous 68165234 10 90222723 90222724 C T 41 GENIC homozygous 68165237 10 90223023 90223024 A G 30 GENIC possibly homozygous 68165240 10 90224161 90224162 C T 31 GENIC homozygous 68165246 10 90224173 90224174 A G 24 GENIC homozygous 68165249 10 90226080 90226081 A G 15 GENIC homozygous 68165256 10 90226696 90226697 T A 29 GENIC possibly homozygous 68455206 10 90227640 90227641 C A 26 GENIC homozygous 68455209 10 90219986 90219987 A T 30 GENIC heterozygous 82695808 10 90233044 90233045 T C 36 GENIC homozygous 68165277