chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 264267132 264267133 A G 9 GENIC homozygous 110441280 2 264267168 264267169 A C 12 GENIC homozygous 120132767 2 264267409 264267410 C T 17 GENIC homozygous 110441281 2 264267517 264267518 A C 16 GENIC homozygous 110441282 2 264267550 264267551 T C 19 GENIC homozygous 110441283 2 264267826 264267827 C T 23 GENIC homozygous 110441284 2 264267972 264267973 A G 20 GENIC homozygous 120132768 2 264268003 264268004 A G 22 GENIC homozygous 110441285 2 264268784 264268785 C T 27 GENIC homozygous 110441286 2 264269097 264269098 G A 26 GENIC homozygous 110441287 2 264269700 264269701 A G 27 GENIC homozygous 110441288 2 264271106 264271107 T C 27 GENIC homozygous 110441289 2 264271201 264271202 A G 14 GENIC homozygous 110441290 2 264271700 264271701 C T 18 GENIC homozygous 110441291 2 264272093 264272094 C T 30 GENIC homozygous 110441292 2 264272097 264272098 G A 30 GENIC homozygous 110441293 2 264272433 264272434 A G 14 GENIC homozygous 110441294 2 264272675 264272676 T C 8 GENIC homozygous 110441295 2 264273650 264273651 A C 31 GENIC possibly homozygous 110441298 2 264273927 264273928 T A 16 GENIC homozygous 110441299 2 264274250 264274251 T C 35 GENIC homozygous 110441300 2 264274547 264274548 A T 33 GENIC homozygous 110441301 2 264274717 264274718 T C 35 GENIC homozygous 110441302