chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 151232967 151232968 T C 15 GENIC homozygous 111776592 3 151234493 151234494 C T 28 GENIC homozygous 111776596 3 151234781 151234782 A G 18 GENIC homozygous 111776598 3 151234912 151234913 T C 26 GENIC homozygous 112431627 3 151235365 151235366 A G 29 GENIC homozygous 111776600 3 151235791 151235792 G C 14 GENIC homozygous 112431628 3 151237769 151237770 C T 26 GENIC homozygous 112431629 3 151239526 151239527 C A 27 GENIC homozygous 112431630 3 151240570 151240571 C T 20 GENIC homozygous 112041535 3 151242187 151242188 G A 16 GENIC homozygous 112431631 3 151243366 151243367 A T 15 GENIC homozygous 112041537 3 151248171 151248172 C T 12 GENIC homozygous 112041539 3 151248227 151248228 T G 10 GENIC homozygous 112431632 3 151250680 151250681 A G 25 GENIC homozygous 111776612 3 151251100 151251101 T G 15 GENIC homozygous 112431633 3 151251428 151251429 A T 23 GENIC homozygous 112431634 3 151251550 151251551 C A 24 GENIC homozygous 112431635 3 151252140 151252141 C T 27 GENIC homozygous 112431636 3 151252215 151252216 C A 35 GENIC homozygous 111776616 3 151252795 151252796 C G 18 GENIC homozygous 112431637 3 151256132 151256133 A G 27 GENIC homozygous 112431638 3 151256328 151256329 G T 7 GENIC homozygous 112431639