chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 74666052 74666053 T A 8 GENIC homozygous 677140502 2 74666392 74666393 G T 4 GENIC homozygous 677140503 2 74667219 74667220 G A 13 GENIC homozygous 677140504 2 74667230 74667231 C CAT 13 GENIC homozygous 772375541 2 74667706 74667707 G A 5 GENIC homozygous 677140505 2 74667953 74667954 T A 10 GENIC homozygous 677140506 2 74668219 74668220 C T 10 GENIC homozygous 677140507 2 74668325 74668326 C T 12 GENIC homozygous 677140508 2 74668344 74668345 G C 13 GENIC homozygous 677140509 2 74668345 74668346 C A 12 GENIC homozygous 677140510 2 74668907 74668908 A G 11 GENIC homozygous 677140511 2 74669081 74669082 T C 3 GENIC homozygous 677140512 2 74669214 74669215 A T 9 GENIC homozygous 677140513 2 74669217 74669218 C T 7 GENIC homozygous 677140514 2 74669330 74669331 C G 6 GENIC homozygous 677140515 2 74669419 74669420 G C 9 GENIC homozygous 677140516 2 74669743 74669744 A G 11 GENIC homozygous 677140517 2 74669852 74669853 T C 3 GENIC homozygous 677140518 2 74670089 74670090 T G 8 GENIC homozygous 677140519 2 74671519 74671520 A C 5 GENIC homozygous 677140520 2 74671965 74671966 C T 11 GENIC homozygous 677140521