chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 167142938 167142939 A G 20 GENIC homozygous 941131989 5 167146882 167146883 C T 30 GENIC homozygous 941131990 5 167148229 167148230 C T 28 GENIC homozygous 941131991 5 167148394 167148395 G A 38 GENIC homozygous 941131992 5 167150122 167150123 T C 14 GENIC homozygous 941131993 5 167150430 167150431 C G 22 GENIC homozygous 941131994 5 167152649 167152650 G T 19 GENIC homozygous 941131995 5 167152650 167152651 T C 19 GENIC homozygous 941131996 5 167153283 167153284 G A 18 GENIC homozygous 941131997 5 167161932 167161933 G A 28 GENIC homozygous 941131998 5 167162385 167162386 G T 15 GENIC homozygous 941131999 5 167162439 167162440 T C 8 GENIC homozygous 941132000 5 167164866 167164867 A G 13 GENIC homozygous 941132001 5 167165856 167165857 G A 9 GENIC homozygous 941132002 5 167167431 167167432 T G 25 GENIC homozygous 941132003 5 167167716 167167717 A G 29 GENIC homozygous 941132004 5 167167948 167167949 G T 26 GENIC homozygous 941132005 5 167167951 167167952 T A 25 GENIC homozygous 941132006 5 167168059 167168060 G T 37 GENIC homozygous 941132007 5 167168071 167168072 C A 38 GENIC homozygous 941132008 5 167169567 167169568 C T 32 GENIC homozygous 941132009 5 167173087 167173088 G T 30 INTERGENIC homozygous 941132010 5 167173790 167173791 A G 26 INTERGENIC homozygous 941132011