chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 59409424 59409425 G C 26 GENIC homozygous 971282340 18 59409466 59409467 C T 26 GENIC homozygous 971282341 18 59409470 59409471 C T 29 GENIC homozygous 971282342 18 59409713 59409714 A G 18 GENIC homozygous 971282343 18 59409716 59409717 C T 20 GENIC homozygous 971282344 18 59410596 59410597 C A 31 GENIC homozygous 971282345 18 59410868 59410869 G A 17 GENIC homozygous 971282346 18 59410952 59410953 T C 35 GENIC homozygous 971282347 18 59411050 59411051 A G 33 GENIC homozygous 971282348 18 59411085 59411086 A G 29 GENIC homozygous 971282349 18 59411508 59411509 C T 31 GENIC homozygous 971282350 18 59412955 59412956 C T 32 GENIC homozygous 971282351 18 59413457 59413458 T A 35 GENIC homozygous 971282352 18 59414673 59414674 T C 31 GENIC homozygous 971282353 18 59416433 59416434 G A 8 GENIC homozygous 971282354 18 59417487 59417488 C T 21 GENIC homozygous 971282355 18 59417833 59417834 T C 37 GENIC homozygous 971282356 18 59417943 59417944 T A 29 GENIC homozygous 971282357