chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 266257617 266257618 G A 39 GENIC homozygous 806126198 1 266259480 266259481 T G 54 GENIC homozygous 806126199 1 266259955 266259956 T C 49 GENIC homozygous 806126200 1 266260071 266260072 A C 73 GENIC homozygous 806126201 1 266260704 266260705 G A 40 GENIC possibly homozygous 806126202 1 266260846 266260847 T A 35 GENIC homozygous 806126203 1 266261396 266261397 G C 50 GENIC homozygous 806126204 1 266262051 266262052 T C 25 GENIC possibly homozygous 806126205 1 266262303 266262304 A G 44 GENIC homozygous 806126206 1 266262580 266262581 C T 49 GENIC homozygous 806126207 1 266263068 266263069 C A 52 GENIC possibly homozygous 806126208 1 266264337 266264338 T A 57 GENIC homozygous 806126209 1 266264589 266264590 A G 48 GENIC homozygous 806126210 1 266265228 266265229 A G 37 GENIC homozygous 806126211 1 266266414 266266415 G T 24 GENIC homozygous 806126212 1 266266712 266266713 C T 50 GENIC homozygous 806126213 1 266267954 266267955 T C 37 GENIC homozygous 806126214 1 266268309 266268310 G A 48 GENIC possibly homozygous 806126215 1 266270325 266270326 A G 28 GENIC homozygous 806126216