chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 264267005 264267006 T C 11 GENIC homozygous 984644707 2 264267132 264267133 A G 14 GENIC homozygous 984644708 2 264267168 264267169 A C 21 GENIC homozygous 984644709 2 264267409 264267410 C T 16 GENIC homozygous 984644710 2 264267517 264267518 A C 21 GENIC homozygous 984644711 2 264267550 264267551 T C 12 GENIC homozygous 984644712 2 264267826 264267827 C T 27 GENIC homozygous 984644713 2 264267972 264267973 A G 20 GENIC homozygous 984644714 2 264268003 264268004 A G 23 GENIC homozygous 984644715 2 264268784 264268785 C T 28 GENIC homozygous 984644716 2 264269097 264269098 G A 32 GENIC homozygous 984644717 2 264269700 264269701 A G 30 GENIC homozygous 984644718 2 264271106 264271107 T C 17 GENIC homozygous 984644719 2 264271201 264271202 A G 10 GENIC homozygous 984644720 2 264271700 264271701 C T 25 GENIC homozygous 984644721 2 264272433 264272434 A G 11 GENIC homozygous 984644722 2 264272675 264272676 T C 11 GENIC homozygous 984644723 2 264273650 264273651 A C 23 GENIC homozygous 984644724 2 264274250 264274251 T C 25 GENIC homozygous 984644725 2 264274547 264274548 A T 12 GENIC homozygous 984644726 2 264274717 264274718 T C 24 GENIC homozygous 984644727