chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 123900994 123900995 A G 5 GENIC homozygous 984022981 X 123901333 123901334 T C 6 GENIC homozygous 984022982 X 123901666 123901667 C A 6 GENIC homozygous 984022983 X 123902771 123902772 C T 8 GENIC homozygous 984022984 X 123903040 123903041 C T 15 GENIC homozygous 984022985 X 123903719 123903720 T A 10 GENIC homozygous 984022986 X 123905627 123905628 A G 4 GENIC homozygous 984022987 X 123906932 123906933 T A 8 GENIC homozygous 984022988 X 123907599 123907600 C T 10 GENIC homozygous 984022989 X 123909136 123909137 C G 7 GENIC homozygous 984022990 X 123911461 123911462 G T 11 INTERGENIC homozygous 984022991 X 123911482 123911483 G A 13 INTERGENIC homozygous 984022992 X 123911483 123911484 T G 14 INTERGENIC homozygous 984022993 X 123912197 123912198 T C 15 INTERGENIC homozygous 984022994 X 123914613 123914614 A G 6 INTERGENIC homozygous 984022995 X 123916196 123916197 A G 12 INTERGENIC homozygous 984022996 X 123916552 123916553 G A 11 INTERGENIC homozygous 984022997 X 123916936 123916937 A G 5 INTERGENIC homozygous 984022998