chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 233991319 233991320 C T 47 GENIC homozygous 61808711 1 233991325 233991326 G T 49 GENIC homozygous 61607963 1 233991565 233991566 T C 22 GENIC homozygous 61607964 1 233992985 233992986 T C 48 GENIC homozygous 61607965 1 233994309 233994310 G A 41 GENIC homozygous 61808712 1 233995324 233995325 C T 47 GENIC homozygous 61607967 1 233995889 233995890 A T 38 GENIC homozygous 61607968 1 233997662 233997663 C G 39 GENIC homozygous 61808713 1 233998311 233998312 C CA 29 GENIC homozygous 61607972 1 233998599 233998601 TG -- 30 GENIC homozygous 61808714 1 233998636 233998637 G T 27 GENIC homozygous 61808715 1 233998710 233998711 G A 25 GENIC possibly homozygous 61607974 1 233999064 233999065 C T 33 GENIC homozygous 61607975 1 233999950 233999955 TGGAT ----- 18 GENIC homozygous 61607976 1 234000509 234000513 AGTC ---- 24 GENIC homozygous 61808716 1 233997361 233997362 T TTG 4 GENIC heterozygous 62203785