chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 142502535 142502536 G A 26 GENIC homozygous 59870378 2 142502778 142502779 A C 25 GENIC homozygous 59870379 2 142503235 142503236 T TG 27 GENIC homozygous 59870380 2 142504354 142504355 G A 37 GENIC homozygous 59870381 2 142505369 142505370 C G 50 GENIC homozygous 59870382 2 142506503 142506504 T C 36 GENIC homozygous 59870383 2 142506688 142506689 A G 40 GENIC homozygous 59870384 2 142506765 142506766 G A 33 GENIC homozygous 59870385 2 142507146 142507147 T A 38 GENIC homozygous 59870386 2 142507395 142507396 G A 28 GENIC heterozygous 59870387 2 142507580 142507581 T C 31 GENIC homozygous 59870388 2 142508985 142508986 C G 10 GENIC homozygous 59870389 2 142509082 142509083 T C 17 GENIC homozygous 59870390 2 142509466 142509467 C T 24 GENIC possibly homozygous 59870391 2 142509737 142509738 T C 35 GENIC homozygous 59870392