chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 267608381 267608382 T C 49 GENIC homozygous 61200961 1 267608865 267608866 G A 46 GENIC homozygous 61200963 1 267609078 267609083 AGTGG ----- 34 GENIC homozygous 61200965 1 267609082 267609083 G GT 35 GENIC heterozygous 61200967 1 267609122 267609123 T - 32 GENIC homozygous 61200969 1 267609168 267609169 G A 46 GENIC possibly homozygous 61200971 1 267609295 267609296 G GC 59 GENIC homozygous 61200973 1 267609303 267609304 T A 60 GENIC homozygous 61200975 1 267609886 267609887 G A 55 GENIC homozygous 61200977 1 267610104 267610105 G A 60 GENIC homozygous 61200979 1 267610445 267610446 A G 44 GENIC homozygous 61200981 1 267610465 267610466 T A 43 GENIC homozygous 61200983 1 267611177 267611179 TT -- 63 GENIC homozygous 61200985 1 267612402 267612403 C T 61 GENIC homozygous 61200987 1 267612680 267612681 A G 72 GENIC homozygous 61200989 1 267613195 267613196 T TTTC 61 GENIC homozygous 61200991 1 267613531 267613532 A T 65 GENIC homozygous 61200993 1 267613647 267613648 G C 69 GENIC homozygous 61200995 1 267613824 267613825 T - 36 GENIC possibly homozygous 61200997 1 267613849 267613850 G GA 44 GENIC homozygous 61200999 1 267614275 267614276 A T 71 GENIC possibly homozygous 61201001 1 267614355 267614356 C T 61 GENIC homozygous 61201003 1 267614367 267614368 C G 58 GENIC homozygous 61201005 1 267615009 267615010 G C 49 GENIC homozygous 61201007 1 267615227 267615228 T - 59 GENIC homozygous 61201009 1 267616354 267616355 G A 70 GENIC possibly homozygous 61201011 1 267616383 267616384 C T 63 GENIC homozygous 61201013 1 267616569 267616570 C T 65 GENIC possibly homozygous 61201015