chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 4771157 4771158 C T 36 GENIC possibly homozygous 71704504 3 4771371 4771372 C T 49 GENIC homozygous 71704507 3 4771390 4771391 A G 44 GENIC homozygous 71704510 3 4773774 4773775 C T 34 GENIC homozygous 71704513 3 4774492 4774493 T C 38 GENIC homozygous 71704516 3 4776805 4776806 C T 51 GENIC homozygous 71704519 3 4778492 4778493 A G 37 GENIC homozygous 71704522 3 4778803 4778804 G A 54 GENIC homozygous 71704525 3 4778958 4778959 A C 36 GENIC homozygous 71704528 3 4779371 4779372 G A 50 GENIC homozygous 71704532 3 4779619 4779620 C A 27 GENIC possibly homozygous 71704535 3 4779750 4779751 A T 38 GENIC homozygous 71704538