chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 44001309 44001310 A C 9 GENIC homozygous 590896471 17 44001922 44001923 G A 11 GENIC heterozygous 590688425 17 44002374 44002375 A G 16 GENIC homozygous 590688426 17 44002437 44002550 ATTGGACTACAGGGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAGAACCAAAAAAA ----------------------------------------------------------------------------------------------------------------- 6 GENIC homozygous 723571220 17 44003309 44003310 A C 18 GENIC possibly homozygous 590688427 17 44004365 44004366 A G 9 GENIC homozygous 590688428 17 44004836 44004837 G A 8 GENIC possibly homozygous 590688429 17 44005006 44005007 A G 11 GENIC homozygous 590688430 17 44005781 44005782 T C 10 GENIC homozygous 590896472 17 44006355 44006356 A G 4 GENIC homozygous 590896473 17 44006970 44006971 C T 13 GENIC homozygous 590896474 17 44007668 44007669 A G 17 GENIC possibly homozygous 590688431 17 44007752 44007753 T TC 15 GENIC homozygous 723571221 17 44009315 44009316 G T 10 GENIC possibly homozygous 590688432 17 44010997 44010998 C T 8 GENIC homozygous 590688433 17 44011412 44011413 T C 13 GENIC homozygous 590688434 17 44013537 44013538 A G 11 GENIC homozygous 590688435 17 44013785 44013786 G A 11 GENIC homozygous 590688436 17 44013884 44013885 G A 15 GENIC possibly homozygous 590688437 17 44017234 44017235 T C 18 GENIC homozygous 590896475 17 44018745 44018746 G A 8 GENIC heterozygous 590688438 17 44019968 44019969 T C 15 GENIC homozygous 590688439 17 44023287 44023288 C G 14 GENIC homozygous 590688440 17 44024222 44024223 C T 9 GENIC homozygous 590896476 17 44025312 44025313 A G 7 GENIC heterozygous 590688441 17 44027124 44027125 T G 15 GENIC possibly homozygous 590688442