chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 44001309 44001310 A C 16 GENIC homozygous 824480026 17 44001922 44001923 G A 16 GENIC homozygous 824480027 17 44002374 44002375 A G 10 GENIC homozygous 824480028 17 44003309 44003310 A C 19 GENIC homozygous 824480029 17 44004365 44004366 A G 16 GENIC homozygous 824480030 17 44004836 44004837 G A 20 GENIC homozygous 824480031 17 44005781 44005782 T C 29 GENIC homozygous 824480032 17 44006355 44006356 A G 13 GENIC homozygous 824480033 17 44006970 44006971 C T 9 GENIC homozygous 824480034 17 44007668 44007669 A G 20 GENIC homozygous 824480035 17 44007752 44007753 T TC 17 GENIC homozygous 824480036 17 44009315 44009316 G T 11 GENIC homozygous 824480037 17 44010997 44010998 C T 12 GENIC homozygous 824480038 17 44011412 44011413 T C 15 GENIC homozygous 824480039 17 44012649 44012653 TTTT ---- 7 GENIC homozygous 824480040 17 44013537 44013538 A G 14 GENIC homozygous 824480041 17 44013785 44013786 G A 17 GENIC homozygous 824480042 17 44013884 44013885 G A 15 GENIC homozygous 824480043 17 44017234 44017235 T C 8 GENIC homozygous 824480044 17 44018745 44018746 G A 22 GENIC homozygous 824480045 17 44019968 44019969 T C 12 GENIC homozygous 824480046 17 44023287 44023288 C G 15 GENIC homozygous 824480047 17 44024222 44024223 C T 12 GENIC homozygous 824480048 17 44025312 44025313 A G 15 GENIC homozygous 824480049 17 44025685 44025686 C CT 13 GENIC homozygous 824480050 17 44027124 44027125 T G 18 GENIC homozygous 824480051