chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 55957081 55957082 A T 21 GENIC homozygous 114553326 13 55958211 55958212 T C 25 GENIC homozygous 114355720 13 55977339 55977340 A C 26 GENIC homozygous 114355732 13 55977365 55977366 T G 31 GENIC homozygous 114355734 13 55977370 55977371 T G 28 GENIC homozygous 114355736 13 55977385 55977386 T C 24 GENIC homozygous 114355738 13 55977453 55977454 T C 33 GENIC homozygous 114355740 13 55977479 55977480 C T 34 GENIC homozygous 114355744 13 55977557 55977558 A G 30 GENIC homozygous 114553328 13 55977850 55977851 G C 22 GENIC homozygous 114355748 13 55977856 55977857 A T 24 GENIC homozygous 114355750 13 55977960 55977961 G T 28 GENIC homozygous 114355752 13 55977962 55977963 A G 25 GENIC homozygous 114355754 13 55977970 55977971 G T 27 GENIC homozygous 114355756 13 55978092 55978093 T G 24 GENIC homozygous 114355758 13 55980290 55980291 G A 22 GENIC homozygous 114553330 13 55980387 55980388 T G 33 GENIC homozygous 114553331 13 55980412 55980413 C T 24 GENIC homozygous 114553332 13 55980484 55980485 A T 34 GENIC homozygous 114553333 13 55980495 55980496 A G 30 GENIC homozygous 114553334 13 55980559 55980560 C T 25 GENIC homozygous 114553335 13 55980580 55980581 C T 25 GENIC homozygous 114553336 13 55980784 55980785 A T 23 GENIC homozygous 114553337 13 55975494 55975495 C A 29 GENIC homozygous 114618310 13 55975887 55975888 C T 16 GENIC homozygous 114618312 13 55978096 55978097 A G 22 GENIC homozygous 114355760 13 55980328 55980329 C T 32 GENIC homozygous 114355762 13 55980879 55980880 C T 32 GENIC homozygous 114553338 13 55980912 55980913 T C 35 GENIC homozygous 114355768 13 55981110 55981111 C T 29 GENIC homozygous 114355774 13 55981232 55981233 G A 38 GENIC homozygous 114355776