chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 9937071 9937072 A G 45 GENIC homozygous 793470488 4 9937075 9937076 T C 44 GENIC homozygous 793470489 4 9937274 9937275 G A 59 GENIC homozygous 793470490 4 9937286 9937287 C T 58 GENIC homozygous 793470491 4 9937298 9937299 G A 52 GENIC homozygous 793470492 4 9937321 9937322 G A 49 GENIC homozygous 793470493 4 9937399 9937400 G A 43 GENIC homozygous 793470494 4 9937460 9937461 C A 41 GENIC homozygous 793470495 4 9937548 9937549 C T 48 GENIC homozygous 793470496 4 9937654 9937655 T G 49 GENIC homozygous 793470497 4 9937701 9937702 G A 52 GENIC homozygous 793470498 4 9937721 9937722 G A 53 GENIC homozygous 793470499 4 9937734 9937735 A C 50 GENIC possibly homozygous 793470500 4 9937746 9937747 A G 51 GENIC homozygous 793470501 4 9937958 9937959 G T 29 GENIC homozygous 793470502 4 9938047 9938048 C G 24 GENIC homozygous 793470503 4 9938175 9938176 A G 34 GENIC homozygous 793470504 4 9938217 9938218 T A 42 GENIC homozygous 793470505 4 9938251 9938252 T A 38 GENIC homozygous 793470506 4 9938416 9938417 C G 36 GENIC homozygous 793470507 4 9938434 9938435 G T 35 GENIC homozygous 793470508 4 9938450 9938451 T C 42 GENIC homozygous 793470509 4 9938482 9938483 G T 45 GENIC possibly homozygous 793470510 4 9938800 9938801 G T 27 GENIC homozygous 793470511 4 9938849 9938850 C T 26 GENIC homozygous 793470512 4 9938879 9938880 A G 24 GENIC homozygous 793470513 4 9938887 9938888 G C 23 GENIC homozygous 793470514