chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 264267005 264267006 T C 24 GENIC homozygous 951897141 2 264267027 264267028 T G 21 GENIC homozygous 951897142 2 264267132 264267133 A G 21 GENIC homozygous 951897143 2 264267168 264267169 A C 25 GENIC homozygous 951897144 2 264267409 264267410 C T 39 GENIC homozygous 951897145 2 264267550 264267551 T C 27 GENIC homozygous 951897146 2 264267826 264267827 C T 18 GENIC homozygous 951897147 2 264267972 264267973 A G 23 GENIC homozygous 951897148 2 264268003 264268004 A G 22 GENIC homozygous 951897149 2 264268784 264268785 C T 25 GENIC homozygous 951897150 2 264269097 264269098 G A 29 GENIC homozygous 951897151 2 264269700 264269701 A G 26 GENIC homozygous 951897152 2 264271106 264271107 T C 27 GENIC homozygous 951897153 2 264271201 264271202 A G 23 GENIC homozygous 951897154 2 264271700 264271701 C T 23 GENIC homozygous 951897155 2 264272433 264272434 A G 18 GENIC homozygous 951897156 2 264272677 264272678 T C 20 GENIC homozygous 951897157 2 264273650 264273651 A C 29 GENIC homozygous 951897158 2 264273927 264273928 T A 22 GENIC homozygous 951897159 2 264274250 264274251 T C 19 GENIC homozygous 951897160 2 264274547 264274548 A T 23 GENIC homozygous 951897161 2 264274717 264274718 T C 24 GENIC homozygous 951897162