chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 7093197 7093198 G A 43 GENIC homozygous 987497460 3 7097542 7097543 G T 26 GENIC homozygous 987497461 3 7098295 7098296 C T 38 GENIC homozygous 987497462 3 7098369 7098370 C T 46 GENIC homozygous 987497463 3 7098610 7098611 T C 31 GENIC homozygous 987497464 3 7099818 7099819 G A 25 GENIC homozygous 987497465 3 7100982 7100983 A G 25 GENIC homozygous 987497466 3 7102967 7102968 G A 21 GENIC homozygous 987497467 3 7104113 7104114 G A 29 GENIC homozygous 987497468 3 7104503 7104504 T C 37 GENIC homozygous 987497469 3 7104695 7104696 C G 23 GENIC homozygous 987497470 3 7105391 7105392 C T 39 GENIC homozygous 987497471 3 7105471 7105472 G T 26 GENIC homozygous 987497472 3 7106196 7106197 A G 42 GENIC homozygous 987497473 3 7107692 7107693 G C 26 GENIC homozygous 987497474 3 7107968 7107969 C T 40 GENIC homozygous 987497475 3 7108363 7108364 T C 32 GENIC homozygous 987497476 3 7109040 7109041 C T 34 GENIC homozygous 987497477 3 7109054 7109055 T C 30 GENIC homozygous 987497478 3 7109119 7109120 C T 30 GENIC homozygous 987497479 3 7109638 7109639 A G 29 GENIC homozygous 987497480 3 7111026 7111027 G A 28 GENIC homozygous 987497481 3 7113120 7113121 C T 23 GENIC homozygous 987497482 3 7114183 7114184 G A 26 GENIC homozygous 987497483 3 7114384 7114385 C T 29 GENIC homozygous 987497484 3 7116979 7116980 A G 31 GENIC homozygous 987497485 3 7117209 7117210 G A 33 GENIC homozygous 987497486 3 7118811 7118812 C G 44 GENIC homozygous 987497487 3 7119476 7119477 G A 30 GENIC homozygous 987497488 3 7121880 7121881 G A 47 GENIC homozygous 987497489 3 7123987 7123988 G A 21 GENIC homozygous 987497490 3 7127362 7127363 A G 40 GENIC homozygous 987497491 3 7128528 7128529 A T 22 GENIC homozygous 987497492