chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 97815625 97815626 G A 21 GENIC homozygous 67126399 13 97816254 97816255 G A 22 GENIC homozygous 67126401 13 97816275 97816276 G A 21 GENIC homozygous 67126403 13 97816320 97816321 C T 14 GENIC homozygous 67126405 13 97817604 97817605 C 20 GENIC homozygous 66881818 13 97817655 97817656 T C 15 GENIC homozygous 66166266 13 97817885 97817886 C T 3 GENIC homozygous 67126407 13 97818491 97818492 T 8 GENIC homozygous 67126409 13 97820945 97820946 A 6 GENIC homozygous 67126411 13 97822347 97822348 G A 17 GENIC heterozygous 67126413 13 97822473 97822474 A G 7 GENIC homozygous 67126415 13 97822505 97822506 A G 13 GENIC homozygous 67126417 13 97822820 97822821 A T 15 GENIC heterozygous 67126419 13 97824082 97824083 T A 23 GENIC homozygous 67126421 13 97824648 97824649 C T 21 GENIC homozygous 67126423 13 97825001 97825002 T 19 GENIC heterozygous 67126425 13 97825243 97825244 A G 7 GENIC homozygous 67126427 13 97827349 97827350 T C 20 GENIC homozygous 67126429 13 97829015 97829015 T 30 GENIC heterozygous 67126431 13 97830481 97830482 G A 26 GENIC homozygous 67126433 13 97830640 97830641 T C 18 GENIC homozygous 67126435 13 97831511 97831512 C T 11 GENIC homozygous 67126437 13 97831779 97831781 CA 16 GENIC homozygous 67126439 13 97832059 97832060 G 8 GENIC homozygous 67126441 13 97832743 97832744 A G 5 GENIC homozygous 67126443 13 97832948 97832949 T C 19 GENIC homozygous 67126445 13 97833078 97833079 T C 27 GENIC homozygous 67126447 13 97833232 97833233 T A 4 GENIC homozygous 67126449 13 97833232 97833233 T 23 GENIC heterozygous 67126451 13 97834462 97834463 A 10 GENIC heterozygous 67126453 13 97834580 97834581 A T 19 GENIC homozygous 67126455 13 97834656 97834657 T C 22 GENIC homozygous 67126457