chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 48276270 48276271 C T 28 GENIC homozygous 113787697 5 48276509 48276510 T C 23 GENIC homozygous 114199433 5 48276711 48276712 A G 27 GENIC homozygous 113787698 5 48277436 48277437 T G 35 GENIC homozygous 113787702 5 48277896 48277897 T C 34 GENIC homozygous 114199434 5 48278203 48278204 A G 32 GENIC homozygous 113787704 5 48280498 48280499 G T 34 GENIC homozygous 114115572 5 48281032 48281033 G T 35 GENIC homozygous 114115574 5 48283906 48283907 G A 35 GENIC homozygous 114199436 5 48283963 48283964 T C 34 GENIC homozygous 113787718 5 48287313 48287314 T C 37 GENIC homozygous 113787725 5 48288063 48288064 C A 31 GENIC homozygous 113787729 5 48288249 48288250 C T 28 GENIC homozygous 114199437 5 48288405 48288406 C T 33 GENIC homozygous 113787732 5 48290671 48290672 T C 30 GENIC homozygous 113787740 5 48290730 48290731 G A 33 GENIC homozygous 114199438 5 48291093 48291094 T C 34 GENIC homozygous 113787742 5 48292006 48292007 C T 22 GENIC homozygous 114199439 5 48292056 48292057 T C 26 GENIC homozygous 114199440