chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6174916 6174917 G T 30 GENIC homozygous 930215955 14 6175198 6175199 T G 35 GENIC possibly homozygous 930215956 14 6175387 6175388 A G 24 GENIC homozygous 930215957 14 6175388 6175389 G A 24 GENIC homozygous 930215958 14 6175517 6175518 T C 25 GENIC homozygous 930215959 14 6177149 6177150 T C 28 GENIC homozygous 930215960 14 6177400 6177401 G C 49 GENIC possibly homozygous 930215961 14 6177456 6177457 T C 52 GENIC homozygous 930215962 14 6177559 6177560 A G 41 GENIC homozygous 930215963 14 6177626 6177627 A G 27 GENIC homozygous 930215964 14 6180114 6180115 G A 15 GENIC homozygous 930215965 14 6218929 6218930 C T 54 GENIC homozygous 930215966 14 6218963 6218964 C G 49 GENIC homozygous 930215967 14 6219311 6219312 C T 37 GENIC homozygous 930215968 14 6219445 6219446 G A 31 GENIC homozygous 930215969 14 6219600 6219601 G A 37 GENIC homozygous 930215970 14 6220214 6220215 C G 21 GENIC homozygous 930215971 14 6220406 6220407 G A 19 GENIC homozygous 930215972 14 6220714 6220715 A G 11 GENIC homozygous 930215973 14 6220981 6220982 A G 25 GENIC homozygous 930215974 14 6221230 6221231 T C 35 GENIC homozygous 930215975