chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 918187 918188 T C 13 GENIC homozygous 109623471 19 918234 918235 A G 11 GENIC homozygous 109623473 19 918373 918374 G A 16 GENIC homozygous 109623475 19 920310 920311 G T 18 GENIC homozygous 109623477 19 921381 921382 T C 27 GENIC homozygous 109623479 19 921568 921569 C T 15 GENIC homozygous 109623481 19 922120 922121 C T 30 GENIC homozygous 109623483 19 924166 924167 A G 25 GENIC homozygous 109623485 19 925435 925436 A T 14 GENIC homozygous 109623487 19 926389 926390 C G 29 GENIC homozygous 109623489 19 930372 930373 A G 24 GENIC homozygous 109623491 19 930960 930961 G A 14 GENIC homozygous 109623493 19 931381 931382 T C 27 GENIC homozygous 109623495 19 931512 931513 G A 24 GENIC homozygous 109623497 19 932531 932532 C T 15 GENIC homozygous 109623499 19 933748 933749 A G 25 GENIC homozygous 109623503 19 933976 933977 G A 22 GENIC homozygous 109623505 19 936334 936335 G A 27 GENIC homozygous 109623507 19 937351 937352 A T 17 GENIC homozygous 109623509 19 937442 937443 T C 15 GENIC homozygous 109623511 19 938960 938961 C G 17 GENIC homozygous 109623513 19 936027 936028 C T 17 GENIC homozygous 109833113