Item | Value |
---|---|
geneid | 2235 |
ensemblid | ENSG00000066926.13 |
hgncid | 3647 |
symbol | FECH |
name | ferrochelatase |
refseq_nuc | NM_000140.5 |
refseq_prot | NP_000131.2 |
ensembl_nuc | ENST00000262093.11 |
ensembl_prot | ENSP00000262093.6 |
mane_status | MANE Select |
chr | chr18 |
start | 57544377 |
end | 57586702 |
strand | - |
ver | v1.2 |
region | chr18:57544377-57586702 |
region5000 | chr18:57539377-57591702 |
regionname0 | FECH_chr18_57544377_57586702 |
regionname5000 | FECH_chr18_57539377_57591702 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 423 | 389 | 80 | 68 | 183 | 15 | 41 | 144 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0002 | 0/0 | 423 | 15 | 5 | 7 | 0 | 1 | 2 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0003 | 0/0 | 423 | 13 | 7 | 2 | 1 | 2 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0004 | 0/0 | 423 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0005 | 0/0 | 423 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0006 | 0/0 | 423 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0007 | 0/0 | 423 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
a0008 | 0/0 | 423 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | MRSLG others(418): Show |
chr18 | 57539377 | 57591702 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1269 | 284 | 78 | 52 | 111 | 9 | 33 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0001c0002 | 1/0 | 1269 | 97 | 2 | 15 | 65 | 6 | 8 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0001c0004 | 0/0 | 1269 | 6 | 0 | 0 | 6 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0001c0011 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0001c0014 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0002c0003 | 0/0 | 1269 | 14 | 5 | 6 | 0 | 1 | 2 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0002c0008 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0003c0005 | 0/0 | 1269 | 6 | 0 | 2 | 1 | 2 | 1 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0003c0006 | 0/0 | 1269 | 6 | 6 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0003c0007 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0004c0012 | 0/0 | 1269 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0005c0009 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0006c0015 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0007c0013 | 0/0 | 1269 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 | ||
a0008c0010 | 0/0 | 1269 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ATGCG others(1264): Show |
chr18 | 57539377 | 57591702 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7692 | 6 | 0 | 2 | 0 | 2 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0003 | 0/0 | 7692 | 11 | 0 | 5 | 3 | 0 | 3 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0005 | 0/0 | 7692 | 9 | 0 | 1 | 8 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0006 | 0/0 | 7692 | 9 | 1 | 3 | 5 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0008 | 0/0 | 7692 | 4 | 0 | 1 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0009 | 0/0 | 7692 | 6 | 6 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0010 | 0/0 | 7691 | 5 | 0 | 0 | 5 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0014 | 0/0 | 7693 | 4 | 1 | 0 | 1 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0015 | 0/0 | 7693 | 5 | 0 | 1 | 4 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0016 | 0/0 | 7693 | 5 | 0 | 4 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0017 | 0/0 | 7692 | 5 | 0 | 1 | 4 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0018 | 0/0 | 7691 | 4 | 2 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0021 | 0/0 | 7692 | 3 | 0 | 1 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0022 | 0/0 | 7689 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0023 | 0/0 | 7693 | 4 | 0 | 1 | 0 | 0 | 3 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0024 | 0/0 | 7694 | 4 | 0 | 0 | 4 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0025 | 0/0 | 7695 | 4 | 1 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0026 | 0/0 | 7692 | 4 | 0 | 2 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0027 | 0/0 | 7693 | 4 | 0 | 3 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0028 | 0/0 | 7691 | 3 | 3 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0029 | 0/0 | 7691 | 2 | 1 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0030 | 0/0 | 7692 | 3 | 1 | 0 | 1 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0035 | 0/0 | 7692 | 2 | 0 | 0 | 0 | 2 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0036 | 0/0 | 7717 | 3 | 1 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7712): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0037 | 0/0 | 7718 | 3 | 0 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7713): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0038 | 0/0 | 7694 | 3 | 0 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0039 | 0/0 | 7717 | 2 | 0 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7712): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0040 | 0/0 | 7689 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0041 | 0/0 | 7690 | 2 | 1 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0042 | 0/0 | 7692 | 2 | 0 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0043 | 0/0 | 7691 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0052 | 0/0 | 7692 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0053 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0054 | 0/0 | 7692 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0055 | 0/0 | 7693 | 2 | 0 | 1 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0056 | 0/0 | 7692 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0057 | 0/0 | 7692 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0058 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0059 | 0/0 | 7692 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0060 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0061 | 0/0 | 7692 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0062 | 0/0 | 7691 | 2 | 0 | 0 | 1 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0063 | 0/0 | 7691 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0064 | 0/0 | 7695 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0065 | 0/0 | 7695 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0066 | 0/0 | 7696 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0067 | 0/0 | 7692 | 2 | 1 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0068 | 0/0 | 7693 | 2 | 0 | 1 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0069 | 0/0 | 7694 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0070 | 0/0 | 7693 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0071 | 0/0 | 7693 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0072 | 0/0 | 7693 | 2 | 0 | 1 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0073 | 0/0 | 7692 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0074 | 0/0 | 7693 | 2 | 0 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0075 | 0/0 | 7693 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0077 | 0/0 | 7693 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0079 | 0/0 | 7689 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0080 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0081 | 0/0 | 7717 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7712): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0082 | 0/0 | 7690 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0083 | 0/0 | 7690 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0088 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0090 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0092 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0093 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0094 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0096 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0098 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0099 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0100 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0102 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0103 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0104 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0105 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0106 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0107 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0108 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0109 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0111 | 0/0 | 7690 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0134 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0135 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0136 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0137 | 0/0 | 7692 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0138 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0139 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0140 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0141 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0142 | 0/1 | 7692 | 1 | 0 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0143 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0144 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0145 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0146 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0147 | 0/0 | 7692 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0148 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0150 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0151 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0152 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0153 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0154 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0155 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0156 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0157 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0158 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0159 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0160 | 0/0 | 7716 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7711): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0161 | 0/0 | 7717 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7712): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0162 | 0/0 | 7717 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7712): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0163 | 0/0 | 7718 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7713): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0164 | 0/0 | 7718 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7713): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0165 | 0/0 | 7718 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7713): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0166 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0167 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0169 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0170 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0171 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0172 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0173 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0174 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0175 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0176 | 0/0 | 7697 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7692): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0177 | 0/0 | 7697 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7692): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0178 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0179 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0180 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0181 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0182 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0183 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0184 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0185 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0186 | 0/0 | 7695 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0187 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0188 | 0/0 | 7695 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0189 | 0/0 | 7696 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0190 | 0/0 | 7695 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0191 | 0/0 | 7695 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7690): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0192 | 0/0 | 7696 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0193 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0194 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0195 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0196 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0197 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0199 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0200 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0201 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0202 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0203 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0204 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0205 | 0/0 | 7693 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0206 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0207 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0208 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0209 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0210 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0211 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0212 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0213 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0214 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0215 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0216 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0217 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0218 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0219 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0220 | 0/0 | 7693 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0222 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0223 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0224 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0225 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0001c0001t0226 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0002 | 0/0 | 7691 | 11 | 0 | 2 | 9 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0004 | 0/0 | 7691 | 6 | 0 | 1 | 4 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0007 | 0/0 | 7691 | 7 | 1 | 0 | 5 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0011 | 0/0 | 7690 | 5 | 0 | 0 | 5 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0012 | 0/0 | 7690 | 4 | 0 | 2 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0013 | 0/0 | 7691 | 5 | 0 | 0 | 5 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0019 | 0/0 | 7690 | 4 | 0 | 0 | 4 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0020 | 0/0 | 7691 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0031 | 0/0 | 7690 | 2 | 0 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0032 | 0/0 | 7688 | 3 | 0 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7683): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0033 | 0/0 | 7691 | 3 | 1 | 1 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0034 | 0/0 | 7692 | 3 | 0 | 0 | 2 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0044 | 0/0 | 7691 | 2 | 0 | 1 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0045 | 0/0 | 7691 | 2 | 0 | 1 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0046 | 0/0 | 7692 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0047 | 0/0 | 7692 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0048 | 0/0 | 7691 | 2 | 0 | 1 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0049 | 0/0 | 7692 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0050 | 0/0 | 7690 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0051 | 0/0 | 7690 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0060 | 0/0 | 7693 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0078 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0085 | 0/0 | 7689 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0086 | 1/0 | 7689 | 1 | 0 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0087 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0112 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0113 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0114 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0115 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0116 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0117 | 0/0 | 7690 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0118 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0119 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0120 | 0/0 | 7691 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0121 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0122 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0123 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0124 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0126 | 0/0 | 7690 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0127 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0128 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0129 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0130 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0131 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0132 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0002t0133 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0004t0021 | 0/0 | 7692 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0001c0004t0022 | 0/0 | 7689 | 3 | 0 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0004t0091 | 0/0 | 7689 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0004t0149 | 0/0 | 7689 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7684): Show |
chr18 | 57539377 | 57591702 |
a0001c0011t0125 | 0/0 | 7691 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0001c0014t0198 | 0/0 | 7692 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0001 | 0/0 | 7692 | 7 | 0 | 6 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0014 | 0/0 | 7693 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7688): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0029 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0066 | 0/0 | 7696 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7691): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0076 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0095 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0097 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0002c0003t0101 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0002c0008t0012 | 0/0 | 7690 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0003c0005t0004 | 0/0 | 7691 | 3 | 0 | 0 | 1 | 2 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0003c0005t0020 | 0/0 | 7691 | 2 | 0 | 1 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0003c0005t0031 | 0/0 | 7690 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7685): Show |
chr18 | 57539377 | 57591702 |
a0003c0006t0008 | 0/0 | 7692 | 3 | 3 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0003c0006t0076 | 0/0 | 7694 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7689): Show |
chr18 | 57539377 | 57591702 |
a0003c0006t0110 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0003c0006t0221 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0003c0007t0084 | 0/0 | 7691 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0004c0012t0053 | 0/0 | 7692 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0005c0009t0058 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0006c0015t0168 | 0/0 | 7692 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
a0007c0013t0089 | 0/0 | 7691 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7686): Show |
chr18 | 57539377 | 57591702 |
a0008c0010t0035 | 0/0 | 7692 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | ACCCG others(7687): Show |
chr18 | 57539377 | 57591702 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0006g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0008g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0009g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0010g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0010g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0010g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0010g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0010g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0014g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0014g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0014g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0014g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0015g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0015g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0016g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0016g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0016g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0016g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0017g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0017g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0017g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0018g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0018g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0018g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0018g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0021g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0021g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0021g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0022g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0023g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0023g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0023g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0023g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0024g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0024g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0024g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0024g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0025g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0025g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0025g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0025g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0026g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0026g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0026g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0026g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0027g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0027g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0027g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0027g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0028g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0028g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0029g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0029g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0030g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0030g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0035g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0035g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0036g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0036g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0036g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0037g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0037g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0038g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0038g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0038g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0039g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0039g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0040g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0040g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0041g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0041g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0042g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0042g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0043g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0052g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0052g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0053g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0054g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0055g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0055g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0056g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0056g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0057g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0057g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0058g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0059g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0059g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0060g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0061g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0062g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0062g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0063g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0063g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0064g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0064g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0065g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0065g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0066g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0067g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0067g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0068g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0068g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0069g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0069g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0070g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0071g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0071g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0072g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0072g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0073g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0073g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0074g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0074g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0075g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0077g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0077g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0079g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0080g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0081g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0082g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0083g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0088g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0090g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0092g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0093g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0094g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0096g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0098g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0099g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0100g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0102g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0103g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0104g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0105g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0106g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0107g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0108g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0109g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0111g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0134g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0135g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0136g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0137g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0138g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0139g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0140g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0141g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0142g0358 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0143g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0144g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0145g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0146g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0147g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0148g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0150g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0151g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0152g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0153g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0154g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0155g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0156g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0157g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0158g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0159g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0160g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0161g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0162g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0163g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0164g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0165g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0166g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0167g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0169g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0170g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0171g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0172g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0173g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0174g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0175g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0176g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0177g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0178g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0179g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0180g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0181g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0182g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0183g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0184g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0185g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0186g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0187g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0188g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0189g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0190g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0191g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0192g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0193g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0194g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0195g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0196g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0197g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0199g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0200g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0201g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0202g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0203g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0204g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0205g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0206g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0207g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0208g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0209g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0210g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0211g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0212g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0213g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0214g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0215g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0216g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0217g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0218g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0219g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0220g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0222g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0223g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0224g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0225g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0001t0226g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0004g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0011g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0011g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0012g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0012g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0012g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0013g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0013g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0013g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0013g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0019g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0019g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0019g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0019g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0020g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0020g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0031g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0031g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0032g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0032g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0033g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0033g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0033g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0034g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0034g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0034g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0044g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0044g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0045g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0045g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0046g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0046g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0047g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0047g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0048g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0048g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0049g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0049g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0050g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0050g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0051g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0051g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0060g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0078g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0085g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0086g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0087g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0112g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0113g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0114g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0115g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0116g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0117g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0118g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0119g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0120g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0121g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0122g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0123g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0124g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0126g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0127g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0128g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0129g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0130g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0131g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0132g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0002t0133g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0004t0021g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0004t0022g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0004t0022g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0004t0022g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0004t0091g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0004t0149g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0011t0125g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0001c0014t0198g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0014g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0029g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0066g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0076g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0095g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0097g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0003t0101g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0002c0008t0012g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0005t0004g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0005t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0005t0020g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0005t0020g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0005t0031g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0006t0008g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0006t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0006t0076g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0006t0110g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0006t0221g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0003c0007t0084g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0004c0012t0053g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0005c0009t0058g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0006c0015t0168g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0007c0013t0089g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
a0008c0010t0035g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0062 | g0132 | EUR | GBR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00140 | hp1 | a0001 | c0002 | t0128 | g0166 | EUR | GBR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00280 | hp1 | a0001 | c0001 | t0080 | g0068 | EUR | FIN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00280 | hp2 | a0001 | c0002 | t0132 | g0167 | EUR | FIN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00323 | hp1 | a0001 | c0002 | t0115 | g0144 | EUR | FIN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00323 | hp2 | a0001 | c0002 | t0131 | g0165 | EUR | FIN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0203 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00438 | hp2 | a0001 | c0001 | t0161 | g0339 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00544 | hp1 | a0001 | c0001 | t0015 | g0129 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00544 | hp2 | a0001 | c0002 | t0013 | g0316 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00558 | hp1 | a0001 | c0001 | t0010 | g0362 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00558 | hp2 | a0001 | c0001 | t0179 | g0122 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00597 | hp1 | a0001 | c0001 | t0066 | g0149 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00597 | hp2 | a0001 | c0002 | t0046 | g0279 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00609 | hp1 | a0001 | c0002 | t0007 | g0212 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00609 | hp2 | a0001 | c0002 | t0007 | g0314 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00639 | hp1 | a0001 | c0001 | t0159 | g0033 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00639 | hp2 | a0001 | c0001 | t0074 | g0148 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00642 | hp1 | a0001 | c0001 | t0096 | g0026 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0387 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00673 | hp1 | a0001 | c0002 | t0004 | g0318 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00673 | hp2 | a0001 | c0001 | t0021 | g0284 | EAS | CHS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00733 | hp2 | a0001 | c0001 | t0042 | g0054 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00735 | hp1 | a0001 | c0002 | t0114 | g0320 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00735 | hp2 | a0001 | c0001 | t0018 | g0192 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00738 | hp1 | a0001 | c0001 | t0108 | g0087 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00741 | hp1 | a0001 | c0001 | t0098 | g0322 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01069 | hp1 | a0001 | c0001 | t0039 | g0083 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01069 | hp2 | a0001 | c0002 | t0012 | g0007 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01070 | hp1 | a0001 | c0001 | t0067 | g0286 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01070 | hp2 | a0001 | c0002 | t0087 | g0150 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01071 | hp1 | a0001 | c0002 | t0012 | g0007 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01071 | hp2 | a0001 | c0001 | t0178 | g0285 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01074 | hp1 | a0001 | c0002 | t0044 | g0246 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01081 | hp1 | a0003 | c0005 | t0020 | g0236 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01081 | hp2 | a0001 | c0002 | t0120 | g0267 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01099 | hp1 | a0001 | c0001 | t0137 | g0045 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0240 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01106 | hp1 | a0001 | c0001 | t0190 | g0049 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01106 | hp2 | a0002 | c0003 | t0001 | g0224 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01109 | hp1 | a0001 | c0001 | t0027 | g0383 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01109 | hp2 | a0001 | c0001 | t0018 | g0196 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01167 | hp1 | a0001 | c0001 | t0195 | g0124 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01167 | hp2 | a0001 | c0001 | t0039 | g0084 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01168 | hp1 | a0001 | c0001 | t0055 | g0032 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01168 | hp2 | a0001 | c0001 | t0192 | g0177 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01175 | hp1 | a0001 | c0002 | t0048 | g0334 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01175 | hp2 | a0001 | c0001 | t0021 | g0069 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01192 | hp1 | a0001 | c0001 | t0026 | g0174 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01192 | hp2 | a0001 | c0001 | t0017 | g0160 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01243 | hp1 | a0004 | c0012 | t0053 | g0055 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01243 | hp2 | a0001 | c0001 | t0029 | g0217 | AMR | PUR | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0173 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0276 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01257 | hp2 | a0001 | c0002 | t0031 | g0169 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01261 | hp2 | a0001 | c0002 | t0078 | g0020 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01346 | hp1 | a0001 | c0001 | t0023 | g0085 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0138 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01358 | hp2 | a0001 | c0001 | t0157 | g0266 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0014 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01433 | hp2 | a0001 | c0002 | t0045 | g0283 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0014 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01496 | hp2 | a0002 | c0008 | t0012 | g0231 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01515 | hp1 | a0001 | c0002 | t0117 | g0143 | EUR | IBS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01515 | hp2 | a0003 | c0005 | t0004 | g0016 | EUR | IBS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01516 | hp1 | a0001 | c0001 | t0035 | g0051 | EUR | IBS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0226 | EUR | IBS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01517 | hp1 | a0001 | c0001 | t0035 | g0050 | EUR | IBS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01517 | hp2 | a0003 | c0005 | t0004 | g0016 | EUR | IBS | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01884 | hp1 | a0001 | c0001 | t0082 | g0191 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01884 | hp2 | a0001 | c0001 | t0174 | g0397 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01891 | hp1 | a0001 | c0001 | t0104 | g0029 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01891 | hp2 | a0001 | c0001 | t0144 | g0046 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01928 | hp1 | a0001 | c0014 | t0198 | g0137 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01928 | hp2 | a0001 | c0002 | t0031 | g0106 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01934 | hp1 | a0001 | c0002 | t0033 | g0301 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01934 | hp2 | a0001 | c0001 | t0042 | g0056 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01943 | hp2 | a0001 | c0001 | t0194 | g0111 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01952 | hp1 | a0001 | c0001 | t0027 | g0198 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01952 | hp2 | a0001 | c0001 | t0016 | g0043 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0041 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01978 | hp2 | a0001 | c0001 | t0072 | g0042 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01981 | hp1 | a0001 | c0001 | t0016 | g0040 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01981 | hp2 | a0001 | c0001 | t0074 | g0114 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01993 | hp1 | a0001 | c0001 | t0006 | g0126 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01993 | hp2 | a0001 | c0001 | t0088 | g0053 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02004 | hp1 | a0001 | c0001 | t0205 | g0037 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02004 | hp2 | a0001 | c0001 | t0027 | g0131 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02015 | hp1 | a0001 | c0002 | t0019 | g0325 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02015 | hp2 | a0001 | c0001 | t0021 | g0304 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02027 | hp1 | a0001 | c0001 | t0164 | g0307 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02027 | hp2 | a0001 | c0002 | t0013 | g0261 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02040 | hp2 | a0001 | c0002 | t0004 | g0145 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02055 | hp1 | a0001 | c0001 | t0175 | g0400 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02055 | hp2 | a0001 | c0001 | t0171 | g0210 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02056 | hp1 | a0001 | c0002 | t0019 | g0309 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02056 | hp2 | a0001 | c0001 | t0081 | g0302 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02074 | hp1 | a0001 | c0001 | t0073 | g0335 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02074 | hp2 | a0001 | c0011 | t0125 | g0281 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02080 | hp1 | a0001 | c0001 | t0025 | g0109 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02083 | hp1 | a0001 | c0001 | t0026 | g0172 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0315 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02129 | hp1 | a0003 | c0005 | t0004 | g0239 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02129 | hp2 | a0001 | c0002 | t0121 | g0346 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02132 | hp1 | a0001 | c0001 | t0030 | g0018 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02132 | hp2 | a0001 | c0001 | t0025 | g0117 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02135 | hp1 | a0001 | c0002 | t0124 | g0163 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02135 | hp2 | a0001 | c0001 | t0182 | g0330 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02145 | hp1 | a0001 | c0001 | t0172 | g0392 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0197 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02148 | hp1 | a0001 | c0001 | t0068 | g0175 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0356 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02155 | hp1 | a0001 | c0001 | t0200 | g0128 | EAS | CDX | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02155 | hp2 | a0001 | c0002 | t0019 | g0058 | EAS | CDX | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02165 | hp1 | a0001 | c0002 | t0013 | g0077 | EAS | CDX | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02165 | hp2 | a0001 | c0002 | t0034 | g0146 | EAS | CDX | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02257 | hp1 | a0001 | c0001 | t0181 | g0399 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02257 | hp2 | a0001 | c0001 | t0186 | g0100 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02258 | hp2 | a0001 | c0001 | t0067 | g0204 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02273 | hp1 | a0001 | c0001 | t0026 | g0095 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02273 | hp2 | a0001 | c0001 | t0015 | g0086 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02280 | hp1 | a0001 | c0001 | t0214 | g0241 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02280 | hp2 | a0001 | c0001 | t0152 | g0071 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0038 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02293 | hp2 | a0003 | c0005 | t0031 | g0235 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0345 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02300 | hp2 | a0001 | c0001 | t0147 | g0183 | AMR | PEL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02451 | hp1 | a0002 | c0003 | t0029 | g0228 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02451 | hp2 | a0001 | c0001 | t0170 | g0105 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02523 | hp1 | a0001 | c0002 | t0046 | g0282 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02523 | hp2 | a0001 | c0002 | t0123 | g0288 | EAS | KHV | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02572 | hp1 | a0001 | c0001 | t0111 | g0030 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02572 | hp2 | a0001 | c0001 | t0177 | g0391 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02602 | hp1 | a0001 | c0001 | t0052 | g0364 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02622 | hp1 | a0001 | c0001 | t0058 | g0395 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0013 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02630 | hp1 | a0001 | c0001 | t0169 | g0047 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02630 | hp2 | a0001 | c0001 | t0222 | g0101 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02647 | hp1 | a0001 | c0001 | t0185 | g0221 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02647 | hp2 | a0001 | c0001 | t0040 | g0257 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02683 | hp1 | a0001 | c0001 | t0136 | g0061 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02683 | hp2 | a0002 | c0003 | t0097 | g0227 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02698 | hp1 | a0001 | c0001 | t0054 | g0005 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02723 | hp1 | a0001 | c0001 | t0153 | g0091 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02723 | hp2 | a0001 | c0001 | t0167 | g0036 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02735 | hp1 | a0001 | c0001 | t0201 | g0152 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02735 | hp2 | a0001 | c0001 | t0059 | g0248 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02738 | hp1 | a0001 | c0001 | t0052 | g0057 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02738 | hp2 | a0001 | c0002 | t0112 | g0361 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02809 | hp1 | a0003 | c0006 | t0076 | g0237 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02809 | hp2 | a0002 | c0003 | t0066 | g0230 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02818 | hp1 | a0001 | c0001 | t0102 | g0195 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02818 | hp2 | a0003 | c0006 | t0110 | g0233 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02886 | hp1 | a0001 | c0001 | t0105 | g0222 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0184 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02895 | hp1 | a0001 | c0001 | t0056 | g0340 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02895 | hp2 | a0001 | c0001 | t0135 | g0025 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02896 | hp1 | a0001 | c0001 | t0213 | g0178 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02896 | hp2 | a0001 | c0001 | t0041 | g0186 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02897 | hp1 | a0001 | c0001 | t0100 | g0189 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02897 | hp2 | a0001 | c0001 | t0056 | g0310 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02922 | hp1 | a0001 | c0001 | t0028 | g0389 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02922 | hp2 | a0001 | c0001 | t0173 | g0396 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02965 | hp1 | a0001 | c0001 | t0083 | g0092 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02965 | hp2 | a0001 | c0001 | t0043 | g0004 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02970 | hp1 | a0001 | c0001 | t0075 | g0011 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02970 | hp2 | a0003 | c0007 | t0084 | g0242 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02976 | hp1 | a0001 | c0001 | t0030 | g0190 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02976 | hp2 | a0001 | c0001 | t0223 | g0102 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03017 | hp1 | a0001 | c0001 | t0143 | g0308 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03017 | hp2 | a0001 | c0001 | t0014 | g0271 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03041 | hp1 | a0001 | c0001 | t0093 | g0103 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03041 | hp2 | a0001 | c0001 | t0014 | g0218 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03098 | hp1 | a0001 | c0001 | t0155 | g0094 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03098 | hp2 | a0001 | c0001 | t0184 | g0070 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03130 | hp1 | a0001 | c0001 | t0166 | g0059 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03130 | hp2 | a0005 | c0009 | t0058 | g0099 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03139 | hp1 | a0001 | c0001 | t0218 | g0220 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03139 | hp2 | a0001 | c0001 | t0099 | g0188 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03195 | hp1 | a0001 | c0001 | t0018 | g0187 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03195 | hp2 | a0001 | c0001 | t0225 | g0194 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03209 | hp1 | a0001 | c0001 | t0043 | g0004 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03209 | hp2 | a0001 | c0001 | t0202 | g0357 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03225 | hp1 | a0001 | c0001 | t0075 | g0011 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03225 | hp2 | a0001 | c0001 | t0040 | g0256 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03239 | hp1 | a0001 | c0002 | t0004 | g0300 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03239 | hp2 | a0001 | c0001 | t0138 | g0034 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03453 | hp1 | a0001 | c0001 | t0094 | g0104 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03453 | hp2 | a0003 | c0006 | t0008 | g0234 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03486 | hp1 | a0002 | c0003 | t0101 | g0229 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03486 | hp2 | a0001 | c0001 | t0063 | g0052 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03490 | hp1 | a0001 | c0001 | t0061 | g0009 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03490 | hp2 | a0001 | c0001 | t0059 | g0264 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03491 | hp1 | a0002 | c0003 | t0014 | g0223 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03491 | hp2 | a0001 | c0001 | t0070 | g0006 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03492 | hp1 | a0001 | c0001 | t0061 | g0009 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03492 | hp2 | a0001 | c0001 | t0070 | g0006 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03516 | hp1 | a0001 | c0001 | t0028 | g0019 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03516 | hp2 | a0001 | c0001 | t0220 | g0393 | AFR | ESN | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03540 | hp1 | a0003 | c0006 | t0221 | g0232 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03540 | hp2 | a0006 | c0015 | t0168 | g0090 | AFR | GWD | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03579 | hp1 | a0003 | c0006 | t0008 | g0015 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03579 | hp2 | a0001 | c0001 | t0176 | g0398 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03654 | hp2 | a0001 | c0001 | t0023 | g0269 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03669 | hp1 | a0001 | c0001 | t0206 | g0182 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03669 | hp2 | a0001 | c0001 | t0151 | g0337 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03688 | hp1 | a0007 | c0013 | t0089 | g0072 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03688 | hp2 | a0001 | c0001 | t0187 | g0062 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03704 | hp1 | a0001 | c0002 | t0007 | g0199 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03704 | hp2 | a0001 | c0002 | t0129 | g0331 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03710 | hp1 | a0001 | c0002 | t0048 | g0299 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03710 | hp2 | a0001 | c0001 | t0154 | g0073 | SAS | PJL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03834 | hp1 | a0001 | c0002 | t0034 | g0200 | SAS | BEB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03834 | hp2 | a0001 | c0001 | t0197 | g0136 | SAS | BEB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03927 | hp1 | a0001 | c0001 | t0023 | g0388 | SAS | BEB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03927 | hp2 | a0001 | c0001 | t0054 | g0005 | SAS | BEB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04115 | hp1 | a0001 | c0001 | t0209 | g0140 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04115 | hp2 | a0001 | c0001 | t0014 | g0365 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0360 | SAS | BEB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04184 | hp2 | a0001 | c0002 | t0133 | g0064 | SAS | BEB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04199 | hp1 | a0001 | c0002 | t0130 | g0060 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04199 | hp2 | a0001 | c0001 | t0023 | g0181 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04204 | hp1 | a0001 | c0001 | t0109 | g0353 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04204 | hp2 | a0003 | c0005 | t0020 | g0238 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG04228 | hp2 | a0008 | c0010 | t0035 | g0035 | SAS | STU | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | YRI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18906 | hp2 | a0001 | c0001 | t0029 | g0390 | AFR | YRI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18939 | hp1 | a0001 | c0001 | t0037 | g0017 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18939 | hp2 | a0001 | c0004 | t0022 | g0368 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18940 | hp1 | a0001 | c0002 | t0047 | g0348 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18940 | hp2 | a0001 | c0001 | t0038 | g0157 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18941 | hp1 | a0001 | c0001 | t0057 | g0268 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18941 | hp2 | a0001 | c0004 | t0149 | g0366 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18943 | hp2 | a0001 | c0002 | t0032 | g0003 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18944 | hp1 | a0001 | c0001 | t0199 | g0155 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18944 | hp2 | a0001 | c0002 | t0126 | g0355 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18945 | hp1 | a0001 | c0001 | t0189 | g0107 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18947 | hp1 | a0001 | c0001 | t0204 | g0273 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18947 | hp2 | a0001 | c0001 | t0057 | g0245 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18949 | hp1 | a0001 | c0001 | t0015 | g0115 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18949 | hp2 | a0001 | c0001 | t0010 | g0382 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18950 | hp1 | a0001 | c0002 | t0020 | g0374 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18950 | hp2 | a0001 | c0001 | t0024 | g0372 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18952 | hp1 | a0001 | c0001 | t0015 | g0329 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18953 | hp1 | a0001 | c0002 | t0049 | g0252 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0250 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18956 | hp1 | a0001 | c0001 | t0065 | g0205 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18956 | hp2 | a0001 | c0001 | t0092 | g0289 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18960 | hp1 | a0001 | c0001 | t0026 | g0088 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18960 | hp2 | a0001 | c0002 | t0085 | g0343 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18961 | hp1 | a0001 | c0002 | t0032 | g0003 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18961 | hp2 | a0001 | c0004 | t0022 | g0386 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0384 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18964 | hp1 | a0001 | c0001 | t0072 | g0274 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18965 | hp1 | a0001 | c0001 | t0022 | g0270 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18966 | hp1 | a0001 | c0001 | t0163 | g0338 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18966 | hp2 | a0001 | c0001 | t0211 | g0133 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18967 | hp1 | a0001 | c0001 | t0210 | g0311 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18967 | hp2 | a0001 | c0002 | t0113 | g0023 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18970 | hp1 | a0001 | c0001 | t0065 | g0108 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18970 | hp2 | a0001 | c0002 | t0118 | g0324 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18971 | hp1 | a0001 | c0001 | t0010 | g0323 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18971 | hp2 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18973 | hp1 | a0001 | c0001 | t0215 | g0130 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18973 | hp2 | a0001 | c0001 | t0165 | g0305 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18975 | hp1 | a0001 | c0002 | t0007 | g0075 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18975 | hp2 | a0001 | c0002 | t0013 | g0342 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18977 | hp1 | a0001 | c0001 | t0216 | g0082 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18977 | hp2 | a0001 | c0002 | t0004 | g0378 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18978 | hp1 | a0001 | c0002 | t0034 | g0151 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18978 | hp2 | a0001 | c0001 | t0207 | g0277 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18979 | hp1 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18979 | hp2 | a0001 | c0002 | t0007 | g0313 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18980 | hp1 | a0001 | c0001 | t0037 | g0017 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18980 | hp2 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18981 | hp1 | a0001 | c0001 | t0077 | g0113 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18981 | hp2 | a0001 | c0001 | t0073 | g0294 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18982 | hp1 | a0001 | c0002 | t0012 | g0373 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18982 | hp2 | a0001 | c0001 | t0017 | g0010 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18983 | hp1 | a0001 | c0001 | t0156 | g0297 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18984 | hp1 | a0001 | c0001 | t0062 | g0121 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18984 | hp2 | a0001 | c0002 | t0044 | g0258 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18986 | hp1 | a0001 | c0001 | t0193 | g0134 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18987 | hp1 | a0001 | c0001 | t0103 | g0385 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18987 | hp2 | a0001 | c0001 | t0226 | g0153 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18989 | hp1 | a0001 | c0001 | t0203 | g0291 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18989 | hp2 | a0001 | c0001 | t0160 | g0154 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18992 | hp1 | a0001 | c0001 | t0024 | g0078 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18992 | hp2 | a0001 | c0001 | t0037 | g0306 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18994 | hp1 | a0001 | c0001 | t0162 | g0376 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18994 | hp2 | a0001 | c0001 | t0068 | g0208 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18997 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18997 | hp2 | a0001 | c0002 | t0060 | g0327 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18998 | hp1 | a0001 | c0001 | t0217 | g0141 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18998 | hp2 | a0001 | c0002 | t0047 | g0377 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18999 | hp1 | a0001 | c0001 | t0038 | g0158 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18999 | hp2 | a0001 | c0004 | t0021 | g0369 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19000 | hp1 | a0001 | c0001 | t0016 | g0211 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19000 | hp2 | a0001 | c0002 | t0050 | g0328 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19002 | hp1 | a0001 | c0001 | t0069 | g0161 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19002 | hp2 | a0001 | c0002 | t0012 | g0350 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19003 | hp1 | a0001 | c0002 | t0020 | g0209 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19003 | hp2 | a0001 | c0002 | t0051 | g0381 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19004 | hp1 | a0001 | c0002 | t0051 | g0326 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19004 | hp2 | a0001 | c0002 | t0119 | g0363 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19005 | hp1 | a0001 | c0001 | t0038 | g0156 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19005 | hp2 | a0001 | c0001 | t0064 | g0097 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19006 | hp1 | a0001 | c0001 | t0036 | g0379 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19006 | hp2 | a0001 | c0001 | t0017 | g0214 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19009 | hp1 | a0001 | c0002 | t0116 | g0375 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19009 | hp2 | a0001 | c0001 | t0196 | g0125 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19010 | hp1 | a0001 | c0001 | t0010 | g0292 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19011 | hp1 | a0001 | c0001 | t0139 | g0162 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0275 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19012 | hp1 | a0001 | c0001 | t0141 | g0244 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19030 | hp1 | a0001 | c0001 | t0145 | g0401 | AFR | LWK | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19030 | hp2 | a0001 | c0001 | t0028 | g0019 | AFR | LWK | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19043 | hp1 | a0001 | c0001 | t0158 | g0093 | AFR | LWK | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | LWK | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19054 | hp1 | a0001 | c0001 | t0071 | g0089 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19054 | hp2 | a0001 | c0004 | t0022 | g0370 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19056 | hp1 | a0001 | c0004 | t0091 | g0367 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19056 | hp2 | a0001 | c0001 | t0008 | g0127 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19058 | hp1 | a0001 | c0002 | t0013 | g0287 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19058 | hp2 | a0001 | c0001 | t0027 | g0251 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19063 | hp1 | a0001 | c0002 | t0011 | g0147 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19063 | hp2 | a0001 | c0002 | t0045 | g0319 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19064 | hp1 | a0001 | c0001 | t0017 | g0010 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19064 | hp2 | a0001 | c0002 | t0050 | g0351 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19065 | hp1 | a0001 | c0001 | t0025 | g0110 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19065 | hp2 | a0001 | c0002 | t0122 | g0262 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19066 | hp2 | a0001 | c0001 | t0036 | g0243 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19067 | hp1 | a0001 | c0002 | t0019 | g0380 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19067 | hp2 | a0001 | c0001 | t0183 | g0176 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19068 | hp1 | a0001 | c0001 | t0208 | g0295 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19068 | hp2 | a0001 | c0001 | t0024 | g0333 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19074 | hp1 | a0001 | c0001 | t0069 | g0201 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19074 | hp2 | a0001 | c0001 | t0008 | g0272 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19076 | hp1 | a0001 | c0001 | t0024 | g0332 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19076 | hp2 | a0001 | c0001 | t0053 | g0303 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19077 | hp2 | a0001 | c0001 | t0010 | g0352 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19079 | hp1 | a0001 | c0001 | t0148 | g0371 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19079 | hp2 | a0001 | c0001 | t0015 | g0112 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19084 | hp1 | a0001 | c0001 | t0014 | g0259 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19084 | hp2 | a0001 | c0001 | t0017 | g0139 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19085 | hp1 | a0001 | c0001 | t0077 | g0159 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19085 | hp2 | a0001 | c0002 | t0007 | g0278 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19086 | hp1 | a0001 | c0001 | t0041 | g0249 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19086 | hp2 | a0001 | c0001 | t0071 | g0120 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19087 | hp2 | a0001 | c0002 | t0049 | g0022 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19088 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19088 | hp2 | a0001 | c0002 | t0032 | g0021 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19089 | hp1 | a0001 | c0002 | t0011 | g0349 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19089 | hp2 | a0001 | c0001 | t0140 | g0336 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19090 | hp1 | a0001 | c0002 | t0127 | g0296 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19090 | hp2 | a0001 | c0001 | t0188 | g0293 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19091 | hp1 | a0001 | c0001 | t0064 | g0096 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19091 | hp2 | a0001 | c0001 | t0060 | g0341 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19240 | hp1 | a0001 | c0001 | t0063 | g0031 | AFR | YRI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA19240 | hp2 | a0001 | c0001 | t0224 | g0185 | AFR | YRI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20129 | hp1 | a0001 | c0002 | t0007 | g0347 | AFR | ASW | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20129 | hp2 | a0001 | c0001 | t0212 | g0179 | AFR | ASW | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20752 | hp1 | a0001 | c0001 | t0090 | g0168 | EUR | TSI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20752 | hp2 | a0001 | c0002 | t0033 | g0317 | EUR | TSI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20805 | hp1 | a0001 | c0001 | t0150 | g0254 | EUR | TSI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20805 | hp2 | a0001 | c0001 | t0055 | g0048 | EUR | TSI | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20905 | hp1 | a0001 | c0001 | t0191 | g0180 | SAS | GIH | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20905 | hp2 | a0001 | c0001 | t0030 | g0018 | SAS | GIH | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0216 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG01123 | hp2 | a0001 | c0001 | t0016 | g0039 | AMR | CLM | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02109 | hp1 | a0001 | c0001 | t0107 | g0193 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02109 | hp2 | a0001 | c0002 | t0033 | g0290 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02486 | hp1 | a0001 | c0001 | t0106 | g0065 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02486 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02559 | hp1 | a0001 | c0001 | t0036 | g0080 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG02559 | hp2 | a0003 | c0006 | t0008 | g0015 | AFR | ACB | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03471 | hp1 | a0001 | c0001 | t0079 | g0219 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG03471 | hp2 | a0001 | c0001 | t0146 | g0081 | AFR | MSL | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG06807 | hp1 | a0002 | c0003 | t0076 | g0225 | AFR | USA | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0394 | AFR | USA | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18955 | hp1 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA18955 | hp2 | a0001 | c0001 | t0180 | g0123 | EAS | JPT | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | USA | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA20300 | hp2 | a0001 | c0001 | t0134 | g0024 | AFR | USA | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA21309 | hp1 | a0001 | c0001 | t0219 | g0028 | AFR | LWK | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
NA21309 | hp2 | a0002 | c0003 | t0095 | g0215 | AFR | LWK | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
homoSapiens | chm13v2 | a0001 | c0001 | t0142 | g0358 | REF | REF | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
homoSapiens | grch38p0 | a0001 | c0002 | t0086 | g0027 | REF | REF | FECH_chr18_57539377_57591702 | FECH | chr18 | 57539377 | 57591702 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:57551319 | G | A | 1 | a0007 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1133C>T | p.Ser378Phe | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 10/11 | 1215/7689 | 1133/1272 | 378/423 | chr18 | 57551319 | |||
chr18:57559148 | C | T | 1 | a0004 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.801G>A | p.Met267Ile | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/11 | 883/7689 | 801/1272 | 267/423 | chr18 | 57559148 | |||
chr18:57566531 | C | T | 1 | a0008 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.514G>A | p.Glu172Lys | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/11 | 596/7689 | 514/1272 | 172/423 | chr18 | 57566531 | |||
chr18:57571460 | A | G | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.395T>C | p.Ile132Thr | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/11 | 477/7689 | 395/1272 | 132/423 | chr18 | 57571460 | |||
chr18:57573273 | C | T | 1 | a0002 | 15 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
missense_variant | MODERATE | c.287G>A | p.Arg96Gln | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/11 | 369/7689 | 287/1272 | 96/423 | chr18 | 57573273 | |||
chr18:57580104 | C | A | 1 | a0003 | 12 | HG01081.hp1 HG01515.hp2 HG01517.hp2 others(9): Show |
missense_variant | MODERATE | c.163G>T | p.Gly55Cys | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/11 | 245/7689 | 163/1272 | 55/423 | chr18 | 57580104 | |||
chr18:57580104 | C | T | 1 | a0003 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.163G>A | p.Gly55Ser | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/11 | 245/7689 | 163/1272 | 55/423 | chr18 | 57580104 | |||
chr18:57580127 | G | C | 1 | a0006 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.140C>G | p.Thr47Arg | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/11 | 222/7689 | 140/1272 | 47/423 | chr18 | 57580127 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:57554416 | T | C | 11 | a0001c0001 a0001c0004 a0001c0014 others(8): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(313): Show |
synonymous_variant | LOW | c.921A>G | p.Pro307Pro | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/11 | 1003/7689 | 921/1272 | 307/423 | chr18 | 57554416 | |||
chr18:57554872 | G | A | 1 | a0001c0011 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.885C>T | p.Asn295Asn | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/11 | 967/7689 | 885/1272 | 295/423 | chr18 | 57554872 | |||
chr18:57554914 | G | A | 1 | a0001c0014 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.843C>T | p.Ser281Ser | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/11 | 925/7689 | 843/1272 | 281/423 | chr18 | 57554914 | |||
chr18:57559151 | G | C | 10 | a0001c0001 a0001c0014 a0002c0003 others(7): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
synonymous_variant | LOW | c.798C>G | p.Pro266Pro | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/11 | 880/7689 | 798/1272 | 266/423 | chr18 | 57559151 | |||
chr18:57580084 | T | C | 1 | a0003c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.183A>G | p.Gln61Gln | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/11 | 265/7689 | 183/1272 | 61/423 | chr18 | 57580084 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:57544534 | C | T | 1 | a0001c0001t0104 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6178G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 6178 | chr18 | 57544534 | ||||||
chr18:57544590 | C | T | 1 | a0001c0002t0121 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6122G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 6122 | chr18 | 57544590 | ||||||
chr18:57544605 | A | G | 37 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0015 others(34): Show |
70 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*6107T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 6107 | chr18 | 57544605 | ||||||
chr18:57544808 | G | A | 20 | a0001c0001t0029 a0001c0001t0052 a0001c0001t0054 others(17): Show |
28 | HG01243.hp2 HG01358.hp2 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5904C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5904 | chr18 | 57544808 | ||||||
chr18:57544811 | A | C | 70 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0014 others(67): Show |
114 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*5901T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5901 | chr18 | 57544811 | ||||||
chr18:57544839 | A | G | 1 | a0001c0002t0131 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5873T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5873 | chr18 | 57544839 | ||||||
chr18:57544889 | T | C | 1 | a0001c0014t0198 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5823A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5823 | chr18 | 57544889 | ||||||
chr18:57544911 | A | C | 2 | a0001c0001t0144 a0001c0001t0186 |
2 | HG01891.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5801T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5801 | chr18 | 57544911 | ||||||
chr18:57545084 | G | T | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0021 others(37): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*5628C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5628 | chr18 | 57545084 | ||||||
chr18:57545124 | C | T | 7 | a0001c0001t0099 a0001c0001t0111 a0001c0001t0145 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5588G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5588 | chr18 | 57545124 | ||||||
chr18:57545318 | C | A | 3 | a0001c0001t0082 a0001c0001t0096 a0002c0003t0095 |
3 | HG00642.hp1 HG01884.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5394G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5394 | chr18 | 57545318 | ||||||
chr18:57545572 | C | T | 1 | a0001c0001t0150 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5140G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5140 | chr18 | 57545572 | ||||||
chr18:57545573 | G | A | 3 | a0001c0001t0082 a0001c0001t0096 a0002c0003t0095 |
3 | HG00642.hp1 HG01884.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5139C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5139 | chr18 | 57545573 | ||||||
chr18:57545664 | G | T | 1 | a0001c0001t0098 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5048C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5048 | chr18 | 57545664 | ||||||
chr18:57545677 | G | A | 1 | a0001c0001t0148 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5035C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 5035 | chr18 | 57545677 | ||||||
chr18:57545741 | T | C | 9 | a0001c0001t0018 a0001c0001t0082 a0001c0001t0083 others(6): Show |
12 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4971A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4971 | chr18 | 57545741 | ||||||
chr18:57545820 | C | CA | 38 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0024 others(35): Show |
58 | HG00323.hp1 HG00597.hp1 HG00733.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*4891dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4891 | chr18 | 57545820 | ||||||
chr18:57545826 | A | C | 30 | a0001c0001t0001 a0001c0001t0029 a0001c0001t0052 others(27): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4886T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4886 | chr18 | 57545826 | ||||||
chr18:57545828 | A | AG | 7 | a0001c0001t0164 a0001c0001t0196 a0001c0001t0215 others(4): Show |
9 | HG00597.hp2 HG02027.hp1 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4883_*4884insC | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4883 | chr18 | 57545828 | ||||||
chr18:57545913 | TTAA | T | 5 | a0001c0001t0022 a0001c0002t0032 a0001c0004t0022 others(2): Show |
9 | NA18939.hp2 NA18941.hp2 NA18943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4796_*4798delTTA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4796 | chr18 | 57545913 | ||||||
chr18:57545978 | C | A | 1 | a0001c0002t0123 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4734G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4734 | chr18 | 57545978 | ||||||
chr18:57546110 | T | C | 1 | a0001c0001t0195 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4602A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4602 | chr18 | 57546110 | ||||||
chr18:57546149 | C | A | 173 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(170): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*4563G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4563 | chr18 | 57546149 | ||||||
chr18:57546249 | T | C | 11 | a0001c0001t0040 a0001c0001t0063 a0001c0001t0075 others(8): Show |
14 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4463A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4463 | chr18 | 57546249 | ||||||
chr18:57546254 | G | A | 2 | a0001c0001t0106 a0001c0001t0107 |
2 | HG02109.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4458C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4458 | chr18 | 57546254 | ||||||
chr18:57546276 | A | G | 1 | a0001c0001t0143 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4436T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4436 | chr18 | 57546276 | ||||||
chr18:57546315 | C | T | 1 | a0001c0002t0119 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4397G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4397 | chr18 | 57546315 | ||||||
chr18:57546345 | G | A | 1 | a0001c0001t0220 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4367C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4367 | chr18 | 57546345 | ||||||
chr18:57546408 | C | T | 1 | a0001c0001t0177 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4304G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4304 | chr18 | 57546408 | ||||||
chr18:57546415 | G | C | 1 | a0001c0001t0061 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4297C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4297 | chr18 | 57546415 | ||||||
chr18:57546606 | T | C | 4 | a0001c0001t0154 a0001c0001t0190 a0001c0001t0191 others(1): Show |
4 | HG01106.hp1 HG01168.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4106A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 4106 | chr18 | 57546606 | ||||||
chr18:57546871 | G | A | 1 | a0001c0001t0155 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3841C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3841 | chr18 | 57546871 | ||||||
chr18:57546959 | C | CA | 53 | a0001c0001t0024 a0001c0001t0036 a0001c0001t0037 others(50): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3752dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3752 | chr18 | 57546959 | ||||||
chr18:57546959 | C | CAA | 12 | a0001c0001t0039 a0001c0001t0108 a0001c0001t0166 others(9): Show |
13 | HG00738.hp1 HG01069.hp1 HG01167.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3751_*3752dupTT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3752 | chr18 | 57546959 | ||||||
chr18:57546959 | C | CAAA | 8 | a0001c0001t0177 a0001c0001t0219 a0001c0001t0220 others(5): Show |
8 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3750_*3752dupTTT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3752 | chr18 | 57546959 | ||||||
chr18:57546959 | CA | C | 6 | a0001c0001t0111 a0001c0001t0134 a0001c0001t0136 others(3): Show |
6 | HG01167.hp1 HG01943.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3752delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3752 | chr18 | 57546959 | ||||||
chr18:57547021 | G | A | 1 | a0001c0011t0125 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3691C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3691 | chr18 | 57547021 | ||||||
chr18:57547111 | T | C | 12 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(9): Show |
17 | HG01069.hp1 HG01167.hp2 HG02027.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3601A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3601 | chr18 | 57547111 | ||||||
chr18:57547145 | C | T | 1 | a0001c0001t0082 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3567G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3567 | chr18 | 57547145 | ||||||
chr18:57547207 | G | T | 1 | a0001c0002t0114 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3505C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3505 | chr18 | 57547207 | ||||||
chr18:57547311 | A | G | 1 | a0001c0001t0092 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3401T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3401 | chr18 | 57547311 | ||||||
chr18:57547335 | C | A | 31 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0018 others(28): Show |
51 | HG00558.hp1 HG00642.hp1 HG00735.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3377G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3377 | chr18 | 57547335 | ||||||
chr18:57547369 | C | A | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3343G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3343 | chr18 | 57547369 | ||||||
chr18:57547373 | C | T | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3339G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3339 | chr18 | 57547373 | ||||||
chr18:57547414 | G | T | 1 | a0001c0002t0128 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3298C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3298 | chr18 | 57547414 | ||||||
chr18:57547542 | A | G | 4 | a0001c0001t0166 a0001c0001t0167 a0001c0001t0169 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3170T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3170 | chr18 | 57547542 | ||||||
chr18:57547583 | G | A | 4 | a0001c0002t0050 a0001c0002t0051 a0001c0002t0126 others(1): Show |
6 | NA18944.hp2 NA19000.hp2 NA19003.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3129C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3129 | chr18 | 57547583 | ||||||
chr18:57547615 | C | G | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3097G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3097 | chr18 | 57547615 | ||||||
chr18:57547671 | C | T | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3041G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 3041 | chr18 | 57547671 | ||||||
chr18:57547973 | A | G | 15 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(12): Show |
20 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2739T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2739 | chr18 | 57547973 | ||||||
chr18:57548228 | G | A | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2484C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2484 | chr18 | 57548228 | ||||||
chr18:57548250 | T | TA | 36 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0016 others(33): Show |
59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*2461dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2461 | chr18 | 57548250 | ||||||
chr18:57548250 | T | TAAA | 22 | a0001c0001t0025 a0001c0001t0064 a0001c0001t0065 others(19): Show |
27 | HG00597.hp1 HG01106.hp1 HG01168.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2459_*2461dupTTT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2461 | chr18 | 57548250 | ||||||
chr18:57548250 | TA | T | 6 | a0001c0001t0040 a0001c0001t0166 a0001c0001t0167 others(3): Show |
7 | HG02630.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2461delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2461 | chr18 | 57548250 | ||||||
chr18:57548261 | A | C | 4 | a0001c0001t0063 a0001c0001t0111 a0001c0001t0141 others(1): Show |
5 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2451T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2451 | chr18 | 57548261 | ||||||
chr18:57548266 | C | A | 60 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(57): Show |
113 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2446G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2446 | chr18 | 57548266 | ||||||
chr18:57548269 | A | C | 2 | a0001c0001t0182 a0001c0001t0183 |
2 | HG02135.hp2 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2443T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2443 | chr18 | 57548269 | ||||||
chr18:57548271 | C | A | 5 | a0001c0001t0073 a0001c0001t0209 a0001c0001t0210 others(2): Show |
6 | HG02074.hp1 HG02976.hp2 HG04115.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2441G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2441 | chr18 | 57548271 | ||||||
chr18:57548341 | A | C | 16 | a0001c0001t0035 a0001c0001t0042 a0001c0001t0052 others(13): Show |
21 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2371T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2371 | chr18 | 57548341 | ||||||
chr18:57548469 | T | G | 1 | a0001c0001t0181 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2243 | chr18 | 57548469 | ||||||
chr18:57548581 | G | A | 2 | a0001c0001t0063 a0001c0001t0111 |
3 | HG02572.hp1 HG03486.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2131C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 2131 | chr18 | 57548581 | ||||||
chr18:57548797 | C | A | 2 | a0001c0001t0017 a0001c0001t0211 |
6 | HG01192.hp2 NA18966.hp2 NA18982.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1915G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1915 | chr18 | 57548797 | ||||||
chr18:57548806 | A | T | 1 | a0001c0002t0113 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1906 | chr18 | 57548806 | ||||||
chr18:57548962 | G | A | 2 | a0001c0001t0212 a0001c0001t0213 |
2 | HG02896.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1750C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1750 | chr18 | 57548962 | ||||||
chr18:57549090 | A | G | 10 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(7): Show |
15 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1622T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1622 | chr18 | 57549090 | ||||||
chr18:57549204 | C | T | 1 | a0001c0002t0112 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1508G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1508 | chr18 | 57549204 | ||||||
chr18:57549233 | A | G | 3 | a0001c0001t0079 a0001c0001t0134 a0001c0001t0135 |
3 | HG02895.hp2 HG03471.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1479T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1479 | chr18 | 57549233 | ||||||
chr18:57549423 | C | CT | 16 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(13): Show |
23 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1288dupA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1288 | chr18 | 57549423 | ||||||
chr18:57549424 | T | TA | 47 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0007 others(44): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1287dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1287 | chr18 | 57549424 | ||||||
chr18:57549424 | T | TTA | 59 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0018 others(56): Show |
81 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1287_*1288insTA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1287 | chr18 | 57549424 | ||||||
chr18:57549424 | T | TTAA | 105 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(102): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1287_*1288insTTA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1287 | chr18 | 57549424 | ||||||
chr18:57549424 | T | TTAAA | 9 | a0001c0001t0027 a0001c0001t0038 a0001c0001t0074 others(6): Show |
15 | HG00639.hp2 HG01109.hp1 HG01952.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1287_*1288insTTTA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1287 | chr18 | 57549424 | ||||||
chr18:57549425 | A | T | 2 | a0001c0001t0079 a0001c0001t0160 |
2 | HG03471.hp1 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1287 | chr18 | 57549425 | ||||||
chr18:57549535 | T | TTTA | 10 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(7): Show |
15 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177insTAA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1176 | chr18 | 57549535 | ||||||
chr18:57549538 | A | AGAGAGTA others(15): Show |
10 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(7): Show |
15 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1173_*1174insCTTC others(18): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1173 | chr18 | 57549538 | ||||||
chr18:57549539 | T | A | 10 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(7): Show |
15 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1173A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1173 | chr18 | 57549539 | ||||||
chr18:57549542 | A | T | 10 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(7): Show |
15 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1170T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 1170 | chr18 | 57549542 | ||||||
chr18:57549776 | G | A | 1 | a0001c0001t0158 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 936 | chr18 | 57549776 | ||||||
chr18:57549820 | A | G | 2 | a0001c0001t0075 a0001c0001t0218 |
3 | HG02970.hp1 HG03139.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*892T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 892 | chr18 | 57549820 | ||||||
chr18:57549997 | C | T | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 715 | chr18 | 57549997 | ||||||
chr18:57550016 | G | A | 9 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(6): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*696C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 696 | chr18 | 57550016 | ||||||
chr18:57550041 | C | T | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 671 | chr18 | 57550041 | ||||||
chr18:57550141 | C | T | 4 | a0001c0001t0166 a0001c0001t0167 a0001c0001t0169 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*571G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 571 | chr18 | 57550141 | ||||||
chr18:57550167 | G | A | 1 | a0001c0001t0159 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 545 | chr18 | 57550167 | ||||||
chr18:57550231 | T | C | 9 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(6): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*481A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 481 | chr18 | 57550231 | ||||||
chr18:57550284 | G | A | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 428 | chr18 | 57550284 | ||||||
chr18:57550289 | C | T | 1 | a0001c0001t0080 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 423 | chr18 | 57550289 | ||||||
chr18:57550290 | A | T | 9 | a0001c0001t0036 a0001c0001t0037 a0001c0001t0039 others(6): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*422T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 422 | chr18 | 57550290 | ||||||
chr18:57550365 | C | T | 1 | a0001c0001t0079 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*347G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 347 | chr18 | 57550365 | ||||||
chr18:57550464 | G | A | 87 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(84): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*248C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 248 | chr18 | 57550464 | ||||||
chr18:57550595 | G | A | 11 | a0001c0001t0075 a0001c0001t0218 a0001c0001t0219 others(8): Show |
12 | HG02630.hp2 HG02809.hp1 HG02970.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*117C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 117 | chr18 | 57550595 | ||||||
chr18:57550615 | T | G | 2 | a0001c0001t0077 a0001c0001t0226 |
3 | NA18981.hp1 NA18987.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*97A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 11/11 | 97 | chr18 | 57550615 | ||||||
chr18:57586635 | C | G | 1 | a0001c0002t0078 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/11 | 15 | chr18 | 57586635 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:57550907 | C | T | 10 | a0001c0001t0001g0253 a0001c0001t0063g0031 a0001c0001t0063g0052 others(7): Show |
11 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1138-61G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 10/10 | chr18 | 57550907 | |||||||
chr18:57551124 | G | A | 2 | a0001c0001t0075g0011 a0001c0001t0218g0220 |
3 | HG02970.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1137+191C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 10/10 | chr18 | 57551124 | |||||||
chr18:57551131 | A | G | 1 | a0001c0001t0036g0243 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1137+184T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 10/10 | chr18 | 57551131 | |||||||
chr18:57551185 | G | T | 2 | a0001c0002t0115g0144 a0001c0002t0117g0143 |
2 | HG00323.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1137+130C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 10/10 | chr18 | 57551185 | |||||||
chr18:57551294 | C | T | 1 | a0002c0008t0012g0231 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1137+21G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 10/10 | chr18 | 57551294 | |||||||
chr18:57551424 | CT | C | 18 | a0001c0001t0042g0054 a0001c0001t0042g0056 a0001c0001t0052g0057 others(15): Show |
19 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1078-51delA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551424 | |||||||
chr18:57551585 | C | T | 1 | a0001c0001t0155g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1078-211G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551585 | |||||||
chr18:57551624 | G | A | 2 | a0001c0001t0024g0332 a0001c0001t0024g0333 |
2 | NA19068.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1078-250C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551624 | |||||||
chr18:57551638 | C | T | 1 | a0001c0001t0079g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1078-264G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551638 | |||||||
chr18:57551815 | T | A | 2 | a0001c0001t0039g0083 a0001c0001t0039g0084 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1078-441A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551815 | |||||||
chr18:57551887 | C | CT | 5 | a0001c0001t0038g0157 a0001c0001t0155g0094 a0001c0001t0170g0105 others(2): Show |
6 | HG02451.hp2 HG03098.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-514dupA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551887 | |||||||
chr18:57551887 | C | CTT | 16 | a0001c0001t0025g0394 a0001c0001t0166g0059 a0001c0001t0167g0036 others(13): Show |
16 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-515_1078-514d others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551887 | |||||||
chr18:57551920 | G | C | 1 | a0001c0002t0002g0076 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1078-546C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551920 | |||||||
chr18:57551949 | T | C | 1 | a0001c0001t0079g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1078-575A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57551949 | |||||||
chr18:57552017 | G | A | 1 | a0001c0001t0220g0393 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1078-643C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552017 | |||||||
chr18:57552103 | C | T | 89 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0354 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.1078-729G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552103 | |||||||
chr18:57552104 | G | A | 1 | a0001c0001t0024g0332 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1078-730C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552104 | |||||||
chr18:57552131 | G | A | 4 | a0001c0001t0166g0059 a0001c0001t0167g0036 a0001c0001t0169g0047 others(1): Show |
4 | HG02630.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-757C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552131 | |||||||
chr18:57552144 | G | A | 299 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(296): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1078-770C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552144 | |||||||
chr18:57552173 | C | T | 1 | a0001c0002t0013g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1078-799G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552173 | |||||||
chr18:57552303 | T | A | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1078-929A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552303 | |||||||
chr18:57552303 | T | C | 2 | a0001c0001t0224g0185 a0001c0001t0225g0194 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078-929A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552303 | |||||||
chr18:57552320 | T | C | 1 | a0001c0001t0024g0333 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1078-946A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552320 | |||||||
chr18:57552453 | T | G | 1 | a0003c0005t0004g0016 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1078-1079A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552453 | |||||||
chr18:57552997 | G | A | 63 | a0001c0001t0001g0255 a0001c0001t0003g0260 a0001c0001t0003g0359 others(60): Show |
65 | HG00639.hp1 HG00673.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.1077+1263C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57552997 | |||||||
chr18:57553151 | G | C | 2 | a0001c0001t0075g0011 a0001c0001t0218g0220 |
3 | HG02970.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1077+1109C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553151 | |||||||
chr18:57553219 | T | TGCTGCAA others(272): Show |
8 | a0001c0001t0036g0243 a0001c0001t0036g0379 a0001c0001t0037g0017 others(5): Show |
9 | HG02027.hp1 NA18939.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077+1040_1077+104 others(283): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553219 | |||||||
chr18:57553219 | T | TGCTGCAA others(272): Show |
2 | a0001c0001t0039g0083 a0001c0001t0039g0084 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1077+1040_1077+104 others(283): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553219 | |||||||
chr18:57553219 | T | TGCTGCAA others(273): Show |
3 | a0001c0001t0036g0080 a0001c0001t0161g0339 a0001c0001t0163g0338 |
3 | HG00438.hp2 HG02559.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1077+1040_1077+104 others(284): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553219 | |||||||
chr18:57553323 | T | A | 1 | a0001c0001t0167g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1077+937A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553323 | |||||||
chr18:57553427 | G | T | 1 | a0001c0002t0020g0209 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1077+833C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553427 | |||||||
chr18:57553675 | G | A | 1 | a0001c0001t0017g0139 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1077+585C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553675 | |||||||
chr18:57553716 | G | A | 1 | a0001c0001t0054g0005 | 2 | HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1077+544C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553716 | |||||||
chr18:57553764 | T | C | 241 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(238): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1077+496A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553764 | |||||||
chr18:57553842 | A | G | 2 | a0001c0002t0114g0320 a0001c0002t0120g0267 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1077+418T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553842 | |||||||
chr18:57553981 | G | A | 1 | a0001c0001t0205g0037 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1077+279C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57553981 | |||||||
chr18:57554008 | A | G | 97 | a0001c0001t0005g0001 a0001c0001t0005g0119 a0001c0001t0005g0170 others(94): Show |
101 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.1077+252T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57554008 | |||||||
chr18:57554136 | GAGGACAC | G | 10 | a0001c0001t0001g0253 a0001c0001t0063g0031 a0001c0001t0063g0052 others(7): Show |
11 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1077+117_1077+123d others(9): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57554136 | |||||||
chr18:57554197 | T | C | 1 | a0001c0001t0212g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1077+63A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57554197 | |||||||
chr18:57554225 | G | A | 11 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(8): Show |
12 | HG00438.hp2 HG02027.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1077+35C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 9/10 | chr18 | 57554225 | |||||||
chr18:57554467 | T | G | 13 | a0001c0001t0025g0394 a0001c0001t0079g0219 a0001c0001t0170g0105 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.913-43A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554467 | |||||||
chr18:57554470 | C | T | 1 | a0001c0002t0046g0282 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.913-46G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554470 | |||||||
chr18:57554484 | CCT | C | 18 | a0001c0001t0042g0054 a0001c0001t0042g0056 a0001c0001t0052g0057 others(15): Show |
19 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.913-62_913-61delAG | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554484 | |||||||
chr18:57554644 | A | G | 1 | a0001c0001t0160g0154 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.912+201T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554644 | |||||||
chr18:57554686 | T | C | 1 | a0001c0001t0025g0394 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.912+159A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554686 | |||||||
chr18:57554698 | G | A | 7 | a0001c0001t0027g0131 a0001c0001t0027g0198 a0001c0001t0027g0383 others(4): Show |
7 | HG00639.hp2 HG01109.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.912+147C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554698 | |||||||
chr18:57554722 | G | C | 1 | a0001c0001t0027g0383 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.912+123C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554722 | |||||||
chr18:57554730 | A | G | 1 | a0001c0001t0026g0174 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.912+115T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554730 | |||||||
chr18:57554748 | C | T | 6 | a0001c0002t0002g0142 a0001c0002t0004g0118 a0001c0002t0007g0314 others(3): Show |
6 | HG00609.hp2 HG02129.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.912+97G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554748 | |||||||
chr18:57554751 | A | T | 46 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0354 others(43): Show |
49 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.912+94T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 8/10 | chr18 | 57554751 | |||||||
chr18:57555008 | C | A | 1 | a0001c0001t0140g0336 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.805-56G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555008 | |||||||
chr18:57555186 | T | C | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-234A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555186 | |||||||
chr18:57555199 | G | A | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.805-247C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555199 | |||||||
chr18:57555487 | C | T | 1 | a0001c0001t0071g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.805-535G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555487 | |||||||
chr18:57555491 | A | G | 14 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(11): Show |
15 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.805-539T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555491 | |||||||
chr18:57555628 | A | G | 2 | a0003c0006t0008g0015 a0003c0006t0008g0234 |
3 | HG02559.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.805-676T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555628 | |||||||
chr18:57555636 | C | A | 1 | a0001c0001t0083g0092 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.805-684G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555636 | |||||||
chr18:57555658 | A | G | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-706T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555658 | |||||||
chr18:57555854 | C | T | 1 | a0001c0004t0149g0366 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.805-902G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57555854 | |||||||
chr18:57556064 | A | G | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1112T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556064 | |||||||
chr18:57556128 | C | T | 46 | a0001c0001t0001g0263 a0001c0001t0009g0012 a0001c0001t0009g0013 others(43): Show |
50 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.805-1176G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556128 | |||||||
chr18:57556145 | A | G | 13 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(10): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.805-1193T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556145 | |||||||
chr18:57556437 | G | C | 1 | a0001c0001t0164g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.805-1485C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556437 | |||||||
chr18:57556468 | G | A | 3 | a0001c0001t0109g0353 a0001c0002t0007g0199 a0001c0002t0034g0200 |
3 | HG03704.hp1 HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.805-1516C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556468 | |||||||
chr18:57556477 | G | A | 2 | a0001c0001t0134g0024 a0001c0001t0135g0025 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.805-1525C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556477 | |||||||
chr18:57556495 | C | T | 1 | a0001c0001t0079g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.805-1543G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556495 | |||||||
chr18:57556636 | C | T | 34 | a0001c0001t0001g0255 a0001c0001t0003g0260 a0001c0001t0003g0359 others(31): Show |
35 | HG00673.hp2 HG01346.hp1 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.805-1684G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556636 | |||||||
chr18:57556664 | G | A | 195 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0003g0260 others(192): Show |
203 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.805-1712C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556664 | |||||||
chr18:57556760 | T | C | 13 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(10): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.805-1808A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556760 | |||||||
chr18:57556838 | T | C | 1 | a0001c0001t0055g0048 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.805-1886A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556838 | |||||||
chr18:57556843 | C | T | 11 | a0001c0001t0018g0187 a0001c0001t0018g0192 a0001c0001t0018g0196 others(8): Show |
11 | HG00735.hp2 HG01109.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.805-1891G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556843 | |||||||
chr18:57556905 | T | C | 58 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0003g0260 others(55): Show |
60 | HG00639.hp1 HG00673.hp2 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.805-1953A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556905 | |||||||
chr18:57556910 | CA | C | 144 | a0001c0001t0006g0138 a0001c0001t0009g0012 a0001c0001t0009g0013 others(141): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.805-1959delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556910 | |||||||
chr18:57556910 | CAA | C | 114 | a0001c0001t0001g0253 a0001c0001t0005g0001 a0001c0001t0005g0119 others(111): Show |
119 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.805-1960_805-1959d others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556910 | |||||||
chr18:57556910 | CAAA | C | 86 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0255 others(83): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.805-1961_805-1959d others(5): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556910 | |||||||
chr18:57556910 | CAAAA | C | 27 | a0001c0001t0003g0298 a0001c0001t0036g0080 a0001c0001t0036g0379 others(24): Show |
29 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.805-1962_805-1959d others(6): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556910 | |||||||
chr18:57556910 | CAAAAA | C | 5 | a0001c0001t0036g0243 a0001c0001t0043g0004 a0001c0001t0096g0026 others(2): Show |
6 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-1963_805-1959d others(7): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556910 | |||||||
chr18:57556984 | G | A | 1 | a0001c0002t0078g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.805-2032C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57556984 | |||||||
chr18:57557094 | G | A | 2 | a0001c0001t0010g0362 a0001c0001t0041g0249 |
2 | HG00558.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.804+2051C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557094 | |||||||
chr18:57557113 | G | C | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2032C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557113 | |||||||
chr18:57557202 | C | T | 1 | a0001c0001t0092g0289 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.804+1943G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557202 | |||||||
chr18:57557300 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.804+1845T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557300 | |||||||
chr18:57557314 | G | C | 1 | a0001c0001t0016g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.804+1831C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557314 | |||||||
chr18:57557408 | G | A | 2 | a0001c0001t0224g0185 a0001c0001t0225g0194 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.804+1737C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557408 | |||||||
chr18:57557582 | T | G | 1 | a0001c0001t0074g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.804+1563A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557582 | |||||||
chr18:57557649 | T | A | 2 | a0001c0001t0040g0256 a0001c0001t0040g0257 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.804+1496A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557649 | |||||||
chr18:57557666 | G | A | 3 | a0001c0001t0014g0271 a0001c0001t0014g0365 a0001c0001t0059g0264 |
3 | HG03017.hp2 HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.804+1479C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557666 | |||||||
chr18:57557705 | G | A | 2 | a0001c0001t0039g0083 a0001c0001t0039g0084 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.804+1440C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557705 | |||||||
chr18:57557736 | A | G | 1 | a0001c0001t0081g0302 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.804+1409T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557736 | |||||||
chr18:57557978 | G | A | 11 | a0001c0001t0075g0011 a0001c0001t0218g0220 a0001c0001t0219g0028 others(8): Show |
12 | HG02630.hp2 HG02809.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.804+1167C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57557978 | |||||||
chr18:57558083 | G | A | 13 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(10): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.804+1062C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558083 | |||||||
chr18:57558122 | C | T | 2 | a0001c0001t0052g0057 a0001c0001t0138g0034 |
2 | HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.804+1023G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558122 | |||||||
chr18:57558133 | T | C | 3 | a0001c0001t0018g0196 a0001c0001t0075g0011 a0001c0001t0218g0220 |
4 | HG01109.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+1012A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558133 | |||||||
chr18:57558218 | T | C | 1 | a0001c0002t0131g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.804+927A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558218 | |||||||
chr18:57558248 | C | T | 13 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(10): Show |
14 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.804+897G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558248 | |||||||
chr18:57558305 | ACAACAGC others(3): Show |
A | 1 | a0001c0001t0006g0384 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.804+830_804+839del others(10): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558305 | |||||||
chr18:57558477 | G | A | 6 | a0001c0002t0002g0074 a0001c0002t0002g0076 a0001c0002t0002g0207 others(3): Show |
6 | NA18953.hp1 NA18975.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.804+668C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558477 | |||||||
chr18:57558545 | T | C | 259 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(256): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.804+600A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558545 | |||||||
chr18:57558763 | T | C | 1 | a0001c0002t0047g0377 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.804+382A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558763 | |||||||
chr18:57558866 | A | G | 17 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(14): Show |
18 | HG00438.hp2 HG01069.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.804+279T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558866 | |||||||
chr18:57558882 | T | C | 30 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(27): Show |
30 | HG00597.hp1 HG01106.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.804+263A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558882 | |||||||
chr18:57558920 | C | CA | 228 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(225): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.804+224dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558920 | |||||||
chr18:57558927 | A | T | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+218T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57558927 | |||||||
chr18:57559022 | T | C | 228 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(225): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.804+123A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57559022 | |||||||
chr18:57559055 | T | C | 2 | a0001c0001t0184g0070 a0001c0001t0185g0221 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.804+90A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 7/10 | chr18 | 57559055 | |||||||
chr18:57559320 | T | C | 11 | a0001c0001t0036g0080 a0001c0001t0036g0243 a0001c0001t0036g0379 others(8): Show |
12 | HG00438.hp2 HG02027.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-77A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559320 | |||||||
chr18:57559362 | G | A | 1 | a0001c0001t0071g0120 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.706-119C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559362 | |||||||
chr18:57559441 | A | G | 204 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(201): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.706-198T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559441 | |||||||
chr18:57559500 | C | T | 2 | a0001c0002t0047g0348 a0001c0002t0047g0377 |
2 | NA18940.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.706-257G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559500 | |||||||
chr18:57559621 | A | T | 2 | a0001c0001t0075g0011 a0001c0001t0218g0220 |
3 | HG02970.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.706-378T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559621 | |||||||
chr18:57559826 | C | G | 218 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(215): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.706-583G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559826 | |||||||
chr18:57559879 | A | G | 247 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(244): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.706-636T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559879 | |||||||
chr18:57559904 | C | T | 3 | a0001c0001t0003g0098 a0001c0001t0003g0247 a0001c0001t0003g0298 |
3 | HG00738.hp2 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.706-661G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559904 | |||||||
chr18:57559951 | G | A | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-708C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559951 | |||||||
chr18:57559969 | G | A | 1 | a0001c0002t0002g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.706-726C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57559969 | |||||||
chr18:57560004 | C | T | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-761G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560004 | |||||||
chr18:57560009 | G | T | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.706-766C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560009 | |||||||
chr18:57560015 | T | C | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-772A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560015 | |||||||
chr18:57560064 | A | G | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.706-821T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560064 | |||||||
chr18:57560099 | A | G | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.706-856T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560099 | |||||||
chr18:57560141 | T | C | 1 | a0001c0001t0069g0201 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.706-898A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560141 | |||||||
chr18:57560172 | G | C | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.706-929C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560172 | |||||||
chr18:57560218 | G | C | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-975C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560218 | |||||||
chr18:57560361 | C | T | 2 | a0001c0002t0002g0356 a0001c0002t0007g0347 |
2 | HG02148.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.706-1118G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560361 | |||||||
chr18:57560377 | G | A | 97 | a0001c0001t0005g0001 a0001c0001t0005g0119 a0001c0001t0005g0170 others(94): Show |
101 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.706-1134C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560377 | |||||||
chr18:57560409 | G | A | 1 | a0001c0001t0211g0133 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.706-1166C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560409 | |||||||
chr18:57560426 | C | T | 97 | a0001c0001t0005g0001 a0001c0001t0005g0119 a0001c0001t0005g0170 others(94): Show |
101 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.706-1183G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560426 | |||||||
chr18:57560438 | C | A | 1 | a0001c0001t0017g0139 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.706-1195G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560438 | |||||||
chr18:57560466 | C | T | 1 | a0001c0001t0071g0120 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.706-1223G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560466 | |||||||
chr18:57560490 | C | A | 233 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.706-1247G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560490 | |||||||
chr18:57560557 | G | A | 1 | a0001c0001t0207g0277 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.706-1314C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560557 | |||||||
chr18:57560606 | G | A | 37 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(34): Show |
38 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.706-1363C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560606 | |||||||
chr18:57560796 | A | C | 4 | a0001c0001t0144g0046 a0001c0001t0166g0059 a0001c0001t0167g0036 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-1553T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57560796 | |||||||
chr18:57561026 | C | G | 1 | a0001c0002t0002g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.706-1783G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561026 | |||||||
chr18:57561046 | C | T | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.706-1803G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561046 | |||||||
chr18:57561072 | G | A | 1 | a0001c0001t0175g0400 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.705+1802C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561072 | |||||||
chr18:57561140 | C | T | 2 | a0001c0002t0007g0278 a0001c0002t0007g0313 |
2 | NA18979.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.705+1734G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561140 | |||||||
chr18:57561339 | C | A | 1 | a0001c0001t0005g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.705+1535G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561339 | |||||||
chr18:57561457 | G | A | 3 | a0001c0002t0050g0328 a0001c0002t0050g0351 a0001c0002t0127g0296 |
3 | NA19000.hp2 NA19064.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.705+1417C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561457 | |||||||
chr18:57561504 | C | T | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.705+1370G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561504 | |||||||
chr18:57561601 | T | G | 1 | a0001c0002t0002g0164 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.705+1273A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561601 | |||||||
chr18:57561776 | C | T | 1 | a0001c0001t0023g0269 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.705+1098G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561776 | |||||||
chr18:57561794 | G | A | 1 | a0001c0001t0162g0376 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.705+1080C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561794 | |||||||
chr18:57561795 | G | T | 1 | a0001c0001t0030g0018 | 2 | HG02132.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.705+1079C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561795 | |||||||
chr18:57561845 | G | A | 35 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(32): Show |
36 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.705+1029C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561845 | |||||||
chr18:57561862 | A | G | 249 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(246): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.705+1012T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561862 | |||||||
chr18:57561863 | T | A | 5 | a0001c0002t0044g0246 a0001c0002t0044g0258 a0001c0002t0045g0283 others(2): Show |
5 | HG01074.hp1 HG01433.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+1011A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57561863 | |||||||
chr18:57562226 | G | A | 3 | a0001c0002t0031g0106 a0001c0002t0031g0169 a0003c0005t0031g0235 |
3 | HG01257.hp2 HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.705+648C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562226 | |||||||
chr18:57562241 | T | C | 1 | a0001c0001t0151g0337 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.705+633A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562241 | |||||||
chr18:57562270 | G | C | 1 | a0001c0001t0025g0117 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.705+604C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562270 | |||||||
chr18:57562475 | C | T | 2 | a0001c0001t0170g0105 a0001c0001t0171g0210 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.705+399G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562475 | |||||||
chr18:57562518 | A | C | 1 | a0002c0003t0001g0224 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.705+356T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562518 | |||||||
chr18:57562533 | GGTCA | G | 4 | a0001c0001t0144g0046 a0001c0001t0166g0059 a0001c0001t0167g0036 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+337_705+340del others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562533 | |||||||
chr18:57562658 | T | C | 3 | a0001c0001t0073g0294 a0001c0001t0073g0335 a0001c0001t0210g0311 |
3 | HG02074.hp1 NA18967.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.705+216A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562658 | |||||||
chr18:57562663 | T | C | 237 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(234): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.705+211A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562663 | |||||||
chr18:57562679 | T | C | 10 | a0001c0001t0079g0219 a0001c0001t0219g0028 a0001c0001t0220g0393 others(7): Show |
10 | HG02630.hp2 HG02809.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.705+195A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562679 | |||||||
chr18:57562796 | T | C | 1 | a0001c0002t0007g0347 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.705+78A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562796 | |||||||
chr18:57562841 | G | T | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.705+33C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562841 | |||||||
chr18:57562855 | C | G | 2 | a0001c0001t0134g0024 a0001c0001t0135g0025 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.705+19G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 6/10 | chr18 | 57562855 | |||||||
chr18:57563092 | G | C | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-112C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563092 | |||||||
chr18:57563203 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.599-223A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563203 | |||||||
chr18:57563235 | C | T | 233 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.599-255G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563235 | |||||||
chr18:57563398 | G | A | 296 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.599-418C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563398 | |||||||
chr18:57563426 | T | C | 1 | a0001c0001t0184g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.599-446A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563426 | |||||||
chr18:57563495 | G | A | 45 | a0001c0001t0001g0263 a0001c0001t0009g0012 a0001c0001t0009g0013 others(42): Show |
49 | HG00558.hp1 HG00735.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.599-515C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563495 | |||||||
chr18:57563578 | C | CA | 47 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0184 others(44): Show |
50 | HG00323.hp1 HG00558.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.599-599_599-598ins others(1): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563578 | |||||||
chr18:57563579 | C | A | 348 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0255 others(345): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.599-599G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563579 | |||||||
chr18:57563580 | C | A | 47 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0184 others(44): Show |
50 | HG00323.hp1 HG00558.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.599-600G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAA | 15 | a0001c0001t0001g0263 a0001c0001t0009g0213 a0001c0001t0010g0382 others(12): Show |
17 | HG00735.hp2 HG00741.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.599-602_599-601dup others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAA | 10 | a0001c0001t0039g0084 a0001c0001t0059g0264 a0001c0001t0214g0241 others(7): Show |
10 | HG01167.hp2 HG02280.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.599-605_599-601dup others(5): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAA | 36 | a0001c0001t0003g0260 a0001c0001t0003g0359 a0001c0001t0003g0360 others(33): Show |
36 | HG01069.hp1 HG01168.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.599-606_599-601dup others(6): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAAA | 39 | a0001c0001t0001g0116 a0001c0001t0001g0255 a0001c0001t0003g0008 others(36): Show |
41 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.599-607_599-601dup others(7): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAAA others(1): Show |
77 | a0001c0001t0001g0253 a0001c0001t0001g0354 a0001c0001t0003g0044 others(74): Show |
83 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.599-608_599-601dup others(8): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAAA others(2): Show |
50 | a0001c0001t0005g0276 a0001c0001t0005g0312 a0001c0001t0006g0135 others(47): Show |
51 | HG00408.hp2 HG00642.hp2 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.599-609_599-601dup others(9): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAAA others(3): Show |
11 | a0001c0001t0017g0160 a0001c0001t0036g0080 a0001c0001t0037g0017 others(8): Show |
12 | HG00639.hp2 HG01192.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.599-610_599-601dup others(10): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0036g0243 a0001c0001t0160g0154 |
2 | NA18989.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.599-611_599-601dup others(11): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563580 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0036g0379 a0001c0001t0161g0339 a0001c0001t0164g0307 |
3 | HG00438.hp2 HG02027.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.599-612_599-601dup others(12): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563580 | |||||||
chr18:57563583 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.599-603T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563583 | |||||||
chr18:57563584 | A | C | 2 | a0001c0001t0005g0119 a0001c0001t0199g0155 |
2 | NA18944.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.599-604T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563584 | |||||||
chr18:57563585 | A | C | 1 | a0001c0001t0145g0401 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.599-605T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563585 | |||||||
chr18:57563677 | GA | G | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-698delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563677 | |||||||
chr18:57563686 | A | C | 12 | a0001c0001t0075g0011 a0001c0001t0079g0219 a0001c0001t0218g0220 others(9): Show |
13 | HG02630.hp2 HG02809.hp1 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-706T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563686 | |||||||
chr18:57563713 | T | C | 35 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(32): Show |
36 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.599-733A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57563713 | |||||||
chr18:57564055 | T | G | 1 | a0001c0001t0006g0203 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.599-1075A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564055 | |||||||
chr18:57564067 | G | A | 296 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.599-1087C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564067 | |||||||
chr18:57564138 | A | G | 12 | a0001c0001t0075g0011 a0001c0001t0079g0219 a0001c0001t0218g0220 others(9): Show |
13 | HG02630.hp2 HG02809.hp1 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.599-1158T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564138 | |||||||
chr18:57564147 | G | A | 2 | a0001c0001t0001g0354 a0001c0001t0003g0079 |
2 | HG01346.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.599-1167C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564147 | |||||||
chr18:57564169 | C | T | 1 | a0001c0001t0104g0029 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.599-1189G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564169 | |||||||
chr18:57564194 | T | C | 1 | a0001c0001t0184g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.599-1214A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564194 | |||||||
chr18:57564356 | G | C | 1 | a0001c0001t0164g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.599-1376C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564356 | |||||||
chr18:57564368 | T | C | 186 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(183): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.599-1388A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564368 | |||||||
chr18:57564428 | A | G | 1 | a0001c0002t0112g0361 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.599-1448T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564428 | |||||||
chr18:57564488 | T | C | 17 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0354 others(14): Show |
18 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(15): Show |
intron_variant | MODIFIER | c.599-1508A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564488 | |||||||
chr18:57564558 | G | T | 233 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.599-1578C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564558 | |||||||
chr18:57564559 | T | C | 1 | a0001c0001t0153g0091 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.599-1579A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564559 | |||||||
chr18:57564574 | A | G | 2 | a0001c0001t0039g0083 a0001c0001t0039g0084 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.599-1594T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564574 | |||||||
chr18:57564586 | A | G | 35 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(32): Show |
36 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.599-1606T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564586 | |||||||
chr18:57564647 | T | C | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-1667A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564647 | |||||||
chr18:57564730 | G | A | 1 | a0001c0001t0016g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.598+1717C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564730 | |||||||
chr18:57564766 | G | A | 1 | a0001c0001t0207g0277 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.598+1681C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564766 | |||||||
chr18:57564834 | A | G | 3 | a0001c0001t0073g0294 a0001c0001t0073g0335 a0001c0001t0210g0311 |
3 | HG02074.hp1 NA18967.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.598+1613T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564834 | |||||||
chr18:57564929 | C | A | 48 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(45): Show |
50 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.598+1518G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564929 | |||||||
chr18:57564940 | A | C | 1 | a0001c0001t0213g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.598+1507T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564940 | |||||||
chr18:57564983 | G | A | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+1464C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57564983 | |||||||
chr18:57565061 | C | A | 185 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.598+1386G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565061 | |||||||
chr18:57565072 | G | T | 1 | a0001c0001t0106g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.598+1375C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565072 | |||||||
chr18:57565075 | T | C | 18 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(15): Show |
18 | HG00597.hp1 HG01106.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.598+1372A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565075 | |||||||
chr18:57565157 | A | C | 12 | a0001c0001t0025g0394 a0001c0001t0170g0105 a0001c0001t0171g0210 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+1290T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565157 | |||||||
chr18:57565266 | T | C | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+1181A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565266 | |||||||
chr18:57565379 | G | A | 2 | a0001c0001t0075g0011 a0001c0001t0218g0220 |
3 | HG02970.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.598+1068C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565379 | |||||||
chr18:57565525 | G | A | 56 | a0001c0001t0001g0255 a0001c0001t0003g0260 a0001c0001t0003g0359 others(53): Show |
58 | HG00639.hp1 HG00673.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.598+922C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565525 | |||||||
chr18:57565537 | T | C | 99 | a0001c0001t0005g0001 a0001c0001t0005g0119 a0001c0001t0005g0170 others(96): Show |
103 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.598+910A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565537 | |||||||
chr18:57565557 | C | G | 1 | a0001c0002t0033g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.598+890G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565557 | |||||||
chr18:57565558 | A | G | 251 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(248): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.598+889T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565558 | |||||||
chr18:57565572 | GA | G | 14 | a0001c0001t0075g0011 a0001c0001t0079g0219 a0001c0001t0173g0396 others(11): Show |
15 | HG02280.hp1 HG02630.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.598+874delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565572 | |||||||
chr18:57565584 | A | G | 187 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(184): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.598+863T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565584 | |||||||
chr18:57565621 | C | A | 2 | a0001c0001t0039g0083 a0001c0001t0039g0084 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.598+826G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565621 | |||||||
chr18:57565627 | A | G | 1 | a0001c0002t0004g0118 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.598+820T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565627 | |||||||
chr18:57565768 | G | A | 1 | a0001c0001t0186g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.598+679C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565768 | |||||||
chr18:57565808 | G | A | 233 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.598+639C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565808 | |||||||
chr18:57565976 | T | C | 1 | a0001c0001t0137g0045 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.598+471A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57565976 | |||||||
chr18:57566013 | C | T | 13 | a0001c0001t0025g0394 a0001c0001t0145g0401 a0001c0001t0170g0105 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+434G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57566013 | |||||||
chr18:57566115 | G | T | 15 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0354 others(12): Show |
16 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+332C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57566115 | |||||||
chr18:57566146 | C | T | 35 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(32): Show |
36 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.598+301G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57566146 | |||||||
chr18:57566376 | A | G | 1 | a0001c0001t0005g0170 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.598+71T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57566376 | |||||||
chr18:57566411 | G | C | 2 | a0001c0001t0224g0185 a0001c0001t0225g0194 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.598+36C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 5/10 | chr18 | 57566411 | |||||||
chr18:57566621 | C | T | 1 | a0001c0001t0145g0401 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.464-40G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57566621 | |||||||
chr18:57566704 | G | A | 2 | a0001c0001t0172g0392 a0001c0001t0177g0391 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.464-123C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57566704 | |||||||
chr18:57566871 | A | G | 14 | a0001c0001t0075g0011 a0001c0001t0079g0219 a0001c0001t0134g0024 others(11): Show |
15 | HG02630.hp2 HG02809.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.464-290T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57566871 | |||||||
chr18:57566880 | T | A | 38 | a0001c0001t0025g0109 a0001c0001t0025g0110 a0001c0001t0025g0117 others(35): Show |
39 | HG00438.hp2 HG00597.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.464-299A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57566880 | |||||||
chr18:57567058 | C | T | 1 | a0001c0001t0098g0322 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.464-477G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57567058 | |||||||
chr18:57567078 | G | C | 1 | a0001c0001t0214g0241 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.464-497C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57567078 | |||||||
chr18:57567111 | G | A | 1 | a0001c0002t0012g0373 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.464-530C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57567111 | |||||||
chr18:57567113 | C | T | 22 | a0001c0001t0035g0050 a0001c0001t0035g0051 a0001c0001t0042g0054 others(19): Show |
23 | HG00639.hp1 HG00733.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.464-532G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57567113 | |||||||
chr18:57567778 | G | T | 239 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(236): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.464-1197C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57567778 | |||||||
chr18:57567830 | T | C | 1 | a0001c0001t0069g0161 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.464-1249A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57567830 | |||||||
chr18:57568045 | T | C | 257 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(254): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.464-1464A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568045 | |||||||
chr18:57568062 | C | T | 1 | a0001c0001t0218g0220 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.464-1481G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568062 | |||||||
chr18:57568063 | G | A | 4 | a0001c0001t0043g0004 a0001c0001t0096g0026 a0001c0001t0104g0029 others(1): Show |
5 | HG00642.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-1482C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568063 | |||||||
chr18:57568149 | G | A | 11 | a0001c0001t0001g0253 a0001c0001t0063g0031 a0001c0001t0063g0052 others(8): Show |
12 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.464-1568C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568149 | |||||||
chr18:57568208 | G | A | 107 | a0001c0001t0005g0001 a0001c0001t0005g0119 a0001c0001t0005g0170 others(104): Show |
112 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.464-1627C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568208 | |||||||
chr18:57568334 | G | C | 43 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(40): Show |
45 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.464-1753C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568334 | |||||||
chr18:57568441 | A | T | 2 | a0001c0001t0039g0083 a0001c0001t0039g0084 |
2 | HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.464-1860T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568441 | |||||||
chr18:57568463 | A | G | 3 | a0001c0001t0057g0245 a0001c0001t0057g0268 a0001c0001t0081g0302 |
3 | HG02056.hp2 NA18941.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.464-1882T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568463 | |||||||
chr18:57568522 | G | A | 11 | a0001c0001t0001g0253 a0001c0001t0063g0031 a0001c0001t0063g0052 others(8): Show |
12 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.464-1941C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568522 | |||||||
chr18:57568569 | A | G | 257 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(254): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.464-1988T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568569 | |||||||
chr18:57568866 | A | G | 1 | a0001c0001t0073g0335 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.464-2285T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568866 | |||||||
chr18:57568917 | C | T | 10 | a0001c0001t0079g0219 a0001c0001t0219g0028 a0001c0001t0220g0393 others(7): Show |
10 | HG02630.hp2 HG02809.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.464-2336G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568917 | |||||||
chr18:57568929 | G | A | 2 | a0001c0002t0114g0320 a0001c0002t0120g0267 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.464-2348C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568929 | |||||||
chr18:57568929 | G | T | 214 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0003g0260 others(211): Show |
224 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(221): Show |
intron_variant | MODIFIER | c.464-2348C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568929 | |||||||
chr18:57568992 | G | A | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.463+2400C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57568992 | |||||||
chr18:57569063 | G | T | 255 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(252): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.463+2329C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569063 | |||||||
chr18:57569110 | T | G | 302 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(299): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.463+2282A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569110 | |||||||
chr18:57569143 | A | T | 2 | a0001c0001t0134g0024 a0001c0001t0135g0025 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.463+2249T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569143 | |||||||
chr18:57569195 | C | T | 201 | a0001c0001t0001g0255 a0001c0001t0001g0263 a0001c0001t0003g0044 others(198): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.463+2197G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569195 | |||||||
chr18:57569318 | T | G | 14 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0354 others(11): Show |
15 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.463+2074A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569318 | |||||||
chr18:57569568 | G | A | 299 | a0001c0001t0001g0253 a0001c0001t0001g0263 a0001c0001t0001g0354 others(296): Show |
312 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(309): Show |
intron_variant | MODIFIER | c.463+1824C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569568 | |||||||
chr18:57569634 | C | T | 4 | a0001c0001t0155g0094 a0001c0001t0158g0093 a0001c0001t0172g0392 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+1758G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569634 | |||||||
chr18:57569685 | A | T | 1 | a0001c0001t0017g0214 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.463+1707T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569685 | |||||||
chr18:57569837 | CT | C | 6 | a0001c0001t0027g0383 a0001c0001t0072g0042 a0001c0001t0201g0152 others(3): Show |
6 | HG01109.hp1 HG01978.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.463+1554delA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569837 | |||||||
chr18:57569840 | T | C | 1 | a0001c0001t0153g0091 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463+1552A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569840 | |||||||
chr18:57569979 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.463+1413C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57569979 | |||||||
chr18:57570025 | TTGTTGTC others(3): Show |
T | 1 | a0001c0002t0033g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.463+1357_463+1366d others(12): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570025 | |||||||
chr18:57570028 | TTGTCG | T | 10 | a0001c0001t0001g0354 a0001c0001t0028g0019 a0001c0001t0028g0389 others(7): Show |
10 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.463+1359_463+1363d others(7): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570028 | |||||||
chr18:57570028 | TTGTCGTG | T | 3 | a0001c0001t0003g0359 a0001c0001t0092g0289 a0001c0001t0109g0353 |
3 | HG02040.hp1 HG04204.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.463+1357_463+1363d others(9): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570028 | |||||||
chr18:57570028 | TTGTCGTG others(8): Show |
T | 1 | a0001c0001t0204g0273 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.463+1349_463+1363d others(17): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570028 | |||||||
chr18:57570029 | TGTC | T | 27 | a0001c0001t0003g0079 a0001c0001t0003g0247 a0001c0001t0003g0298 others(24): Show |
29 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.463+1360_463+1362d others(5): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570029 | |||||||
chr18:57570031 | T | TG | 21 | a0001c0001t0005g0275 a0001c0001t0008g0272 a0001c0001t0008g0321 others(18): Show |
21 | HG00609.hp2 HG02074.hp1 HG02148.hp2 others(18): Show |
intron_variant | MODIFIER | c.463+1360_463+1361i others(3): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570031 | |||||||
chr18:57570031 | T | TGTG | 3 | a0001c0001t0027g0383 a0001c0001t0140g0336 a0001c0002t0013g0316 |
3 | HG00544.hp2 HG01109.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.463+1360_463+1361i others(5): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570031 | |||||||
chr18:57570031 | TC | T | 34 | a0001c0001t0015g0329 a0001c0001t0024g0078 a0001c0001t0024g0372 others(31): Show |
34 | HG00741.hp1 HG01175.hp1 HG02523.hp2 others(31): Show |
intron_variant | MODIFIER | c.463+1360delG | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570031 | |||||||
chr18:57570032 | C | CGT | 18 | a0001c0001t0006g0250 a0001c0001t0006g0384 a0001c0001t0022g0270 others(15): Show |
18 | HG01074.hp1 HG01433.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.463+1358_463+1359d others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | C | CGTGT | 10 | a0001c0001t0003g0098 a0001c0001t0005g0276 a0001c0001t0021g0284 others(7): Show |
11 | HG00673.hp2 HG00738.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.463+1356_463+1359d others(6): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | C | T | 24 | a0001c0001t0005g0275 a0001c0001t0008g0272 a0001c0001t0008g0321 others(21): Show |
24 | HG00544.hp2 HG00609.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.463+1360G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGT | C | 109 | a0001c0001t0001g0116 a0001c0001t0003g0008 a0001c0001t0003g0067 others(106): Show |
113 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.463+1358_463+1359d others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGT | C | 33 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0009g0012 others(30): Show |
39 | HG01081.hp1 HG01515.hp2 HG01517.hp2 others(36): Show |
intron_variant | MODIFIER | c.463+1356_463+1359d others(6): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGTGT | C | 22 | a0001c0001t0015g0086 a0001c0001t0023g0085 a0001c0001t0025g0394 others(19): Show |
22 | HG00099.hp1 HG01069.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.463+1354_463+1359d others(8): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0096g0026 a0001c0001t0105g0222 a0001c0001t0155g0094 others(1): Show |
4 | HG00642.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+1352_463+1359d others(10): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGTGTG others(3): Show |
C | 1 | a0006c0015t0168g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.463+1350_463+1359d others(12): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGTGTG others(9): Show |
C | 3 | a0001c0001t0036g0243 a0001c0001t0037g0017 a0001c0001t0062g0121 |
4 | NA18939.hp1 NA18980.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+1344_463+1359d others(18): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGTGTG others(11): Show |
C | 3 | a0001c0001t0014g0218 a0001c0001t0061g0009 a0001c0001t0079g0219 |
4 | HG03041.hp2 HG03471.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+1342_463+1359d others(20): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570032 | CGTGTGTG others(21): Show |
C | 34 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(31): Show |
36 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.463+1332_463+1359d others(30): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570032 | |||||||
chr18:57570037 | GTGT | G | 10 | a0001c0001t0023g0181 a0001c0001t0070g0006 a0001c0001t0090g0168 others(7): Show |
11 | HG01168.hp2 HG03491.hp2 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.463+1352_463+1354d others(5): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570037 | |||||||
chr18:57570076 | T | A | 2 | a0002c0003t0029g0228 a0002c0003t0101g0229 |
2 | HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.463+1316A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570076 | |||||||
chr18:57570085 | A | G | 149 | a0001c0001t0001g0253 a0001c0001t0001g0263 a0001c0001t0001g0354 others(146): Show |
153 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.463+1307T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570085 | |||||||
chr18:57570164 | G | T | 38 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(35): Show |
41 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.463+1228C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570164 | |||||||
chr18:57570245 | T | C | 1 | a0001c0001t0074g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.463+1147A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570245 | |||||||
chr18:57570252 | T | C | 17 | a0001c0001t0003g0359 a0001c0001t0015g0329 a0001c0001t0027g0251 others(14): Show |
19 | HG00597.hp1 HG02015.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.463+1140A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570252 | |||||||
chr18:57570484 | T | A | 32 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(29): Show |
35 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.463+908A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570484 | |||||||
chr18:57570533 | T | C | 2 | a0001c0001t0029g0217 a0001c0001t0061g0009 |
3 | HG01243.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.463+859A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570533 | |||||||
chr18:57570636 | T | A | 1 | a0001c0001t0055g0048 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.463+756A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570636 | |||||||
chr18:57570655 | A | T | 17 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(14): Show |
19 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(16): Show |
intron_variant | MODIFIER | c.463+737T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570655 | |||||||
chr18:57570680 | T | C | 17 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(14): Show |
19 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(16): Show |
intron_variant | MODIFIER | c.463+712A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570680 | |||||||
chr18:57570696 | C | T | 44 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(41): Show |
47 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.463+696G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570696 | |||||||
chr18:57570835 | G | A | 1 | a0001c0001t0136g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.463+557C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570835 | |||||||
chr18:57570899 | A | G | 2 | a0001c0001t0134g0024 a0001c0001t0135g0025 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.463+493T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570899 | |||||||
chr18:57570933 | C | T | 4 | a0001c0001t0148g0371 a0001c0004t0022g0368 a0001c0004t0022g0370 others(1): Show |
4 | NA18939.hp2 NA19054.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+459G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57570933 | |||||||
chr18:57571164 | T | G | 2 | a0001c0001t0063g0031 a0001c0001t0063g0052 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.463+228A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57571164 | |||||||
chr18:57571178 | C | CT | 5 | a0001c0001t0001g0255 a0001c0001t0015g0086 a0001c0001t0023g0085 others(2): Show |
5 | HG01069.hp1 HG01167.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+213dupA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57571178 | |||||||
chr18:57571349 | G | A | 12 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.463+43C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 4/10 | chr18 | 57571349 | |||||||
chr18:57571588 | A | G | 94 | a0001c0001t0001g0116 a0001c0001t0005g0001 a0001c0001t0005g0119 others(91): Show |
97 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.315-48T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57571588 | |||||||
chr18:57571627 | G | A | 4 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0184 others(1): Show |
6 | HG02258.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-87C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57571627 | |||||||
chr18:57571819 | A | C | 48 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(45): Show |
52 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.315-279T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57571819 | |||||||
chr18:57571912 | A | C | 5 | a0001c0001t0001g0255 a0001c0001t0015g0086 a0001c0001t0023g0085 others(2): Show |
5 | HG01069.hp1 HG01167.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-372T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57571912 | |||||||
chr18:57572038 | C | T | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.315-498G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572038 | |||||||
chr18:57572065 | G | A | 12 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.315-525C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572065 | |||||||
chr18:57572508 | G | A | 4 | a0001c0001t0014g0218 a0001c0001t0029g0217 a0001c0001t0061g0009 others(1): Show |
5 | HG01243.hp2 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+738C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572508 | |||||||
chr18:57572513 | T | TAAA | 9 | a0001c0001t0025g0394 a0001c0001t0058g0395 a0001c0001t0173g0396 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+730_314+732dup others(3): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572513 | |||||||
chr18:57572513 | TA | T | 283 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0263 others(280): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.314+732delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572513 | |||||||
chr18:57572513 | TAA | T | 26 | a0001c0001t0009g0184 a0001c0001t0015g0086 a0001c0001t0036g0243 others(23): Show |
29 | HG01081.hp1 HG01168.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.314+731_314+732del others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572513 | |||||||
chr18:57572539 | G | T | 1 | a0003c0005t0031g0235 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.314+707C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572539 | |||||||
chr18:57572581 | A | AACG | 32 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(29): Show |
35 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.314+662_314+664dup others(3): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572581 | |||||||
chr18:57572583 | C | T | 1 | a0001c0002t0032g0021 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.314+663G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572583 | |||||||
chr18:57572588 | T | TG | 180 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(177): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.314+657dupC | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572588 | |||||||
chr18:57572588 | T | TGG | 87 | a0001c0001t0001g0354 a0001c0001t0006g0173 a0001c0001t0006g0202 others(84): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.314+656_314+657dup others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572588 | |||||||
chr18:57572588 | TG | T | 36 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(33): Show |
38 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.314+657delC | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572588 | |||||||
chr18:57572628 | C | T | 11 | a0001c0001t0202g0357 a0003c0005t0004g0016 a0003c0005t0004g0239 others(8): Show |
13 | HG01081.hp1 HG01515.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.314+618G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572628 | |||||||
chr18:57572629 | G | A | 2 | a0001c0001t0147g0183 a0001c0001t0154g0073 |
2 | HG02300.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.314+617C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572629 | |||||||
chr18:57572866 | A | AAGAAGGG others(4): Show |
4 | a0001c0001t0014g0218 a0001c0001t0029g0217 a0001c0001t0061g0009 others(1): Show |
5 | HG01243.hp2 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+369_314+379dup others(11): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57572866 | |||||||
chr18:57573223 | T | C | 392 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(389): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.314+23A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 3/10 | chr18 | 57573223 | |||||||
chr18:57573386 | C | T | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195-21G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57573386 | |||||||
chr18:57573459 | C | G | 1 | a0001c0002t0031g0106 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.195-94G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57573459 | |||||||
chr18:57573476 | T | C | 34 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(31): Show |
36 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.195-111A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57573476 | |||||||
chr18:57573604 | C | T | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195-239G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57573604 | |||||||
chr18:57573736 | G | C | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195-371C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57573736 | |||||||
chr18:57573866 | G | C | 30 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(27): Show |
33 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.195-501C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57573866 | |||||||
chr18:57574066 | G | A | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195-701C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574066 | |||||||
chr18:57574091 | G | A | 11 | a0001c0001t0202g0357 a0003c0005t0004g0016 a0003c0005t0004g0239 others(8): Show |
13 | HG01081.hp1 HG01515.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.195-726C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574091 | |||||||
chr18:57574225 | G | A | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195-860C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574225 | |||||||
chr18:57574329 | G | A | 1 | a0001c0001t0006g0384 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.195-964C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574329 | |||||||
chr18:57574482 | G | A | 1 | a0001c0001t0075g0011 | 2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.195-1117C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574482 | |||||||
chr18:57574531 | G | T | 7 | a0001c0001t0008g0038 a0001c0001t0016g0039 a0001c0001t0016g0040 others(4): Show |
7 | HG01123.hp2 HG01952.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-1166C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574531 | |||||||
chr18:57574920 | C | T | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.195-1555G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574920 | |||||||
chr18:57574947 | C | T | 1 | a0001c0001t0186g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.195-1582G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574947 | |||||||
chr18:57574963 | C | T | 390 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(387): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.195-1598G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57574963 | |||||||
chr18:57575012 | C | G | 12 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.195-1647G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57575012 | |||||||
chr18:57575387 | A | G | 12 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.195-2022T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57575387 | |||||||
chr18:57575687 | G | A | 10 | a0001c0001t0005g0170 a0001c0001t0006g0171 a0001c0001t0006g0173 others(7): Show |
10 | HG00609.hp1 HG01192.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.195-2322C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57575687 | |||||||
chr18:57575792 | AG | A | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.195-2428delC | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57575792 | |||||||
chr18:57575927 | C | T | 2 | a0001c0001t0105g0222 a0001c0001t0185g0221 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.195-2562G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57575927 | |||||||
chr18:57575932 | C | T | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.195-2567G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57575932 | |||||||
chr18:57576073 | C | T | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.195-2708G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57576073 | |||||||
chr18:57576079 | T | C | 1 | a0001c0001t0003g0359 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.195-2714A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57576079 | |||||||
chr18:57576094 | C | G | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.195-2729G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57576094 | |||||||
chr18:57576579 | G | A | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.195-3214C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57576579 | |||||||
chr18:57576579 | G | C | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195-3214C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57576579 | |||||||
chr18:57577004 | C | T | 1 | a0001c0001t0106g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.194+3069G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577004 | |||||||
chr18:57577081 | A | G | 6 | a0002c0003t0001g0014 a0002c0003t0001g0216 a0002c0003t0001g0224 others(3): Show |
7 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.194+2992T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577081 | |||||||
chr18:57577113 | G | A | 2 | a0001c0001t0063g0031 a0001c0001t0063g0052 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.194+2960C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577113 | |||||||
chr18:57577132 | C | T | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.194+2941G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577132 | |||||||
chr18:57577322 | CT | C | 33 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(30): Show |
35 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.194+2750delA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577322 | |||||||
chr18:57577342 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.194+2731G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577342 | |||||||
chr18:57577343 | G | A | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.194+2730C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577343 | |||||||
chr18:57577378 | A | T | 3 | a0001c0001t0105g0222 a0001c0001t0185g0221 a0001c0001t0218g0220 |
3 | HG02647.hp1 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.194+2695T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577378 | |||||||
chr18:57577478 | A | G | 1 | a0001c0002t0122g0262 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.194+2595T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577478 | |||||||
chr18:57577540 | C | G | 1 | a0001c0002t0013g0261 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.194+2533G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577540 | |||||||
chr18:57577648 | T | C | 2 | a0001c0001t0105g0222 a0001c0001t0185g0221 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.194+2425A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577648 | |||||||
chr18:57577661 | T | TTA | 47 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.194+2410_194+2411d others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577661 | |||||||
chr18:57577957 | G | GT | 15 | a0001c0001t0146g0081 a0002c0003t0001g0014 a0002c0003t0001g0216 others(12): Show |
16 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.194+2115dupA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577957 | |||||||
chr18:57577965 | TG | T | 11 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.194+2107delC | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577965 | |||||||
chr18:57577966 | G | T | 35 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(32): Show |
39 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.194+2107C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57577966 | |||||||
chr18:57578272 | A | C | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.194+1801T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578272 | |||||||
chr18:57578389 | G | A | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.194+1684C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578389 | |||||||
chr18:57578397 | G | A | 16 | a0001c0001t0014g0218 a0001c0001t0025g0394 a0001c0001t0029g0217 others(13): Show |
17 | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.194+1676C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578397 | |||||||
chr18:57578624 | G | A | 343 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0255 others(340): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.194+1449C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578624 | |||||||
chr18:57578643 | G | A | 1 | a0006c0015t0168g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.194+1430C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578643 | |||||||
chr18:57578758 | G | A | 46 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.194+1315C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578758 | |||||||
chr18:57578796 | C | A | 9 | a0001c0001t0093g0103 a0001c0001t0094g0104 a0001c0001t0170g0105 others(6): Show |
9 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+1277G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578796 | |||||||
chr18:57578833 | C | T | 1 | a0001c0001t0014g0259 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.194+1240G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578833 | |||||||
chr18:57578857 | G | A | 1 | a0001c0001t0162g0376 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.194+1216C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578857 | |||||||
chr18:57578958 | C | CA | 13 | a0001c0001t0023g0181 a0001c0001t0070g0006 a0001c0001t0075g0011 others(10): Show |
15 | HG01168.hp2 HG02300.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.194+1114dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578958 | |||||||
chr18:57578964 | A | T | 1 | a0001c0001t0162g0376 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.194+1109T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578964 | |||||||
chr18:57578977 | C | T | 2 | a0001c0001t0040g0256 a0001c0001t0040g0257 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.194+1096G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57578977 | |||||||
chr18:57579243 | CT | C | 16 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(13): Show |
16 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.194+829delA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579243 | |||||||
chr18:57579244 | T | A | 1 | a0002c0003t0066g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.194+829A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579244 | |||||||
chr18:57579244 | T | C | 65 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0044 others(62): Show |
72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.194+829A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579244 | |||||||
chr18:57579245 | C | A | 66 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0044 others(63): Show |
73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.194+828G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579245 | |||||||
chr18:57579260 | G | T | 1 | a0001c0001t0040g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.194+813C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579260 | |||||||
chr18:57579265 | A | ATATATAT others(13): Show |
41 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0014g0218 others(38): Show |
45 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.194+807_194+808ins others(20): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579265 | |||||||
chr18:57579273 | A | ATGTGTGT others(15): Show |
16 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(13): Show |
16 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.194+799_194+800ins others(22): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579273 | |||||||
chr18:57579275 | G | GTGTGTAT others(27): Show |
14 | a0001c0001t0138g0034 a0002c0003t0001g0014 a0002c0003t0001g0216 others(11): Show |
15 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+797_194+798ins others(34): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579275 | |||||||
chr18:57579279 | G | GTATA | 11 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(8): Show |
13 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(10): Show |
intron_variant | MODIFIER | c.194+793_194+794ins others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579279 | |||||||
chr18:57579281 | G | C | 11 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(8): Show |
13 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(10): Show |
intron_variant | MODIFIER | c.194+792C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579281 | |||||||
chr18:57579283 | G | A | 11 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(8): Show |
13 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(10): Show |
intron_variant | MODIFIER | c.194+790C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579283 | |||||||
chr18:57579285 | A | G | 14 | a0001c0001t0138g0034 a0002c0003t0001g0014 a0002c0003t0001g0216 others(11): Show |
15 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+788T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579285 | |||||||
chr18:57579287 | A | G | 14 | a0001c0001t0138g0034 a0002c0003t0001g0014 a0002c0003t0001g0216 others(11): Show |
15 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+786T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579287 | |||||||
chr18:57579289 | A | ATG | 31 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0184 others(28): Show |
33 | HG00735.hp2 HG00738.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.194+782_194+783dup others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579289 | |||||||
chr18:57579289 | A | ATGTG | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.194+780_194+783dup others(4): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579289 | |||||||
chr18:57579289 | A | G | 22 | a0001c0001t0001g0255 a0001c0001t0003g0260 a0001c0001t0014g0259 others(19): Show |
23 | HG00642.hp2 HG01069.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.194+784T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579289 | |||||||
chr18:57579313 | G | A | 16 | a0001c0001t0003g0360 a0001c0001t0059g0248 a0001c0001t0138g0034 others(13): Show |
17 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.194+760C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTA | 3 | a0001c0001t0029g0217 a0001c0001t0061g0009 a0001c0001t0146g0081 |
4 | HG01243.hp2 HG03471.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+759_194+760ins others(6): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTAT others(1): Show |
11 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.194+759_194+760ins others(8): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTAT others(3): Show |
4 | a0001c0001t0145g0401 a0001c0001t0155g0094 a0001c0001t0158g0093 others(1): Show |
4 | HG03098.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+759_194+760ins others(10): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0153g0091 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.194+759_194+760ins others(12): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTGT others(3): Show |
32 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(29): Show |
34 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.194+759_194+760ins others(10): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTGT others(5): Show |
8 | a0001c0001t0003g0008 a0001c0001t0003g0067 a0001c0001t0021g0069 others(5): Show |
9 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.194+759_194+760ins others(12): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0106g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.194+759_194+760ins others(14): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579313 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0001g0066 a0001c0002t0012g0007 |
3 | HG00140.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.194+759_194+760ins others(14): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579313 | |||||||
chr18:57579315 | A | G | 2 | a0001c0002t0044g0258 a0005c0009t0058g0099 |
2 | HG03130.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.194+758T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579315 | |||||||
chr18:57579348 | A | G | 64 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(61): Show |
67 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.194+725T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579348 | |||||||
chr18:57579429 | G | A | 7 | a0001c0001t0043g0004 a0001c0001t0063g0031 a0001c0001t0063g0052 others(4): Show |
8 | HG00642.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.194+644C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579429 | |||||||
chr18:57579554 | G | A | 151 | a0001c0001t0001g0253 a0001c0001t0001g0263 a0001c0001t0001g0354 others(148): Show |
155 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.194+519C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579554 | |||||||
chr18:57579636 | T | C | 95 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0044 others(92): Show |
104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.194+437A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579636 | |||||||
chr18:57579767 | G | A | 18 | a0001c0001t0009g0012 a0001c0001t0009g0013 a0001c0001t0009g0184 others(15): Show |
20 | HG00735.hp2 HG01109.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.194+306C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579767 | |||||||
chr18:57579774 | C | G | 1 | a0001c0001t0003g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.194+299G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579774 | |||||||
chr18:57579886 | C | T | 14 | a0002c0003t0001g0014 a0002c0003t0001g0216 a0002c0003t0001g0224 others(11): Show |
15 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.194+187G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57579886 | |||||||
chr18:57580030 | G | A | 11 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.194+43C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 2/10 | chr18 | 57580030 | |||||||
chr18:57580222 | G | A | 150 | a0001c0001t0001g0116 a0001c0001t0003g0098 a0001c0001t0005g0001 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.68-23C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580222 | |||||||
chr18:57580279 | T | C | 1 | a0001c0001t0184g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.68-80A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580279 | |||||||
chr18:57580400 | G | A | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.68-201C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580400 | |||||||
chr18:57580442 | C | A | 1 | a0001c0001t0190g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.68-243G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580442 | |||||||
chr18:57580559 | G | GA | 198 | a0001c0001t0001g0116 a0001c0001t0003g0044 a0001c0001t0003g0098 others(195): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.68-361dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580559 | |||||||
chr18:57580583 | G | A | 1 | a0001c0001t0103g0385 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.68-384C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580583 | |||||||
chr18:57580592 | G | A | 1 | a0001c0001t0015g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.68-393C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580592 | |||||||
chr18:57580648 | G | A | 2 | a0001c0001t0025g0394 a0001c0001t0220g0393 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-449C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580648 | |||||||
chr18:57580659 | G | C | 2 | a0001c0001t0150g0254 a0001c0002t0112g0361 |
2 | HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.68-460C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580659 | |||||||
chr18:57580699 | G | T | 1 | a0001c0002t0116g0375 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.68-500C>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580699 | |||||||
chr18:57580779 | A | G | 2 | a0001c0001t0064g0096 a0001c0001t0064g0097 |
2 | NA19005.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.68-580T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580779 | |||||||
chr18:57580809 | C | T | 1 | a0001c0001t0026g0095 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.68-610G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580809 | |||||||
chr18:57580840 | T | C | 4 | a0001c0001t0014g0218 a0001c0001t0029g0217 a0001c0001t0061g0009 others(1): Show |
5 | HG01243.hp2 HG03041.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-641A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580840 | |||||||
chr18:57580856 | C | T | 1 | a0001c0001t0150g0254 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.68-657G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580856 | |||||||
chr18:57580904 | C | A | 1 | a0003c0005t0004g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.68-705G>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57580904 | |||||||
chr18:57581061 | C | T | 3 | a0001c0001t0145g0401 a0001c0001t0155g0094 a0001c0001t0158g0093 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-862G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581061 | |||||||
chr18:57581062 | A | G | 390 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(387): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.68-863T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581062 | |||||||
chr18:57581352 | A | G | 4 | a0001c0001t0042g0054 a0001c0001t0042g0056 a0001c0001t0088g0053 others(1): Show |
4 | HG00733.hp2 HG01243.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1153T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581352 | |||||||
chr18:57581599 | G | A | 1 | a0001c0001t0027g0198 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.68-1400C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581599 | |||||||
chr18:57581658 | G | A | 62 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0044 others(59): Show |
68 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.68-1459C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581658 | |||||||
chr18:57581669 | T | C | 2 | a0001c0002t0007g0199 a0001c0002t0034g0200 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.68-1470A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581669 | |||||||
chr18:57581791 | G | A | 2 | a0001c0001t0010g0362 a0001c0001t0041g0249 |
2 | HG00558.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.68-1592C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581791 | |||||||
chr18:57581904 | G | A | 1 | a0001c0001t0029g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68-1705C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581904 | |||||||
chr18:57581910 | C | T | 36 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(33): Show |
39 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.68-1711G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57581910 | |||||||
chr18:57582006 | T | TA | 35 | a0001c0001t0003g0044 a0001c0001t0008g0038 a0001c0001t0016g0039 others(32): Show |
38 | HG00733.hp2 HG00741.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.68-1808dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582006 | |||||||
chr18:57582006 | TA | T | 16 | a0001c0001t0083g0092 a0001c0001t0096g0026 a0001c0002t0020g0209 others(13): Show |
17 | HG00642.hp1 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-1808delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582006 | |||||||
chr18:57582010 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.68-1811T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582010 | |||||||
chr18:57582025 | T | C | 1 | a0001c0002t0119g0363 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.68-1826A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582025 | |||||||
chr18:57582061 | C | CA | 373 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0001g0253 others(370): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.68-1863_68-1862ins others(1): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582061 | |||||||
chr18:57582084 | C | T | 1 | a0001c0001t0029g0217 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.68-1885G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582084 | |||||||
chr18:57582164 | C | T | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.68-1965G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582164 | |||||||
chr18:57582307 | A | T | 171 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(168): Show |
177 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.68-2108T>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582307 | |||||||
chr18:57582347 | T | C | 1 | a0001c0001t0052g0364 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.68-2148A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582347 | |||||||
chr18:57582354 | G | GT | 13 | a0002c0003t0001g0014 a0002c0003t0001g0216 a0002c0003t0001g0224 others(10): Show |
14 | HG01099.hp2 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-2156dupA | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582354 | |||||||
chr18:57582646 | G | A | 1 | a0001c0001t0014g0365 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68-2447C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582646 | |||||||
chr18:57582695 | C | T | 1 | a0001c0002t0049g0252 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.68-2496G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582695 | |||||||
chr18:57582696 | G | A | 2 | a0001c0001t0134g0024 a0001c0001t0135g0025 |
2 | HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.68-2497C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582696 | |||||||
chr18:57582736 | A | G | 1 | a0001c0001t0153g0091 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.68-2537T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582736 | |||||||
chr18:57582736 | ACC | A | 13 | a0002c0003t0001g0014 a0002c0003t0001g0216 a0002c0003t0001g0224 others(10): Show |
14 | HG01099.hp2 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-2539_68-2538del others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582736 | |||||||
chr18:57582757 | CA | C | 147 | a0001c0001t0001g0116 a0001c0001t0003g0098 a0001c0001t0005g0001 others(144): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.68-2559delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582757 | |||||||
chr18:57582836 | C | T | 150 | a0001c0001t0001g0116 a0001c0001t0003g0098 a0001c0001t0005g0001 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.68-2637G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582836 | |||||||
chr18:57582857 | AGAC | A | 6 | a0001c0001t0015g0086 a0001c0001t0023g0085 a0001c0001t0036g0243 others(3): Show |
7 | HG01069.hp1 HG01167.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-2661_68-2659del others(3): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57582857 | |||||||
chr18:57583032 | T | C | 341 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0255 others(338): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.68-2833A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583032 | |||||||
chr18:57583165 | C | T | 1 | a0001c0001t0027g0251 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.68-2966G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583165 | |||||||
chr18:57583318 | A | G | 1 | a0001c0001t0006g0250 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.68-3119T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583318 | |||||||
chr18:57583438 | G | A | 153 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(150): Show |
157 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.67+3116C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583438 | |||||||
chr18:57583438 | G | C | 1 | a0001c0001t0006g0203 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.67+3116C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583438 | |||||||
chr18:57583504 | G | A | 1 | a0001c0001t0067g0204 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.67+3050C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583504 | |||||||
chr18:57583589 | T | C | 7 | a0001c0001t0148g0371 a0001c0004t0021g0369 a0001c0004t0022g0368 others(4): Show |
7 | NA18939.hp2 NA18941.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+2965A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583589 | |||||||
chr18:57583662 | T | C | 189 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(186): Show |
197 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.67+2892A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583662 | |||||||
chr18:57583665 | A | G | 1 | a0006c0015t0168g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.67+2889T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583665 | |||||||
chr18:57583854 | G | A | 4 | a0001c0001t0035g0050 a0001c0001t0035g0051 a0001c0001t0070g0006 others(1): Show |
5 | HG01516.hp1 HG01517.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+2700C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583854 | |||||||
chr18:57583900 | C | G | 1 | a0001c0001t0071g0089 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.67+2654G>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583900 | |||||||
chr18:57583904 | G | A | 3 | a0001c0001t0152g0071 a0001c0001t0154g0073 a0007c0013t0089g0072 |
3 | HG02280.hp2 HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.67+2650C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583904 | |||||||
chr18:57583919 | T | C | 341 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0255 others(338): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.67+2635A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583919 | |||||||
chr18:57583939 | T | C | 154 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(151): Show |
158 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.67+2615A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57583939 | |||||||
chr18:57584148 | C | T | 1 | a0001c0001t0055g0032 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.67+2406G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584148 | |||||||
chr18:57584168 | G | C | 3 | a0001c0001t0036g0243 a0001c0001t0037g0017 a0003c0007t0084g0242 |
4 | HG02970.hp2 NA18939.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2386C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584168 | |||||||
chr18:57584178 | CA | C | 68 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0044 others(65): Show |
76 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.67+2375delT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584178 | |||||||
chr18:57584178 | CAA | C | 322 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0255 others(319): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.67+2374_67+2375del others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584178 | |||||||
chr18:57584195 | G | C | 150 | a0001c0001t0001g0116 a0001c0001t0003g0098 a0001c0001t0005g0001 others(147): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.67+2359C>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584195 | |||||||
chr18:57584257 | T | C | 1 | a0001c0002t0020g0374 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.67+2297A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584257 | |||||||
chr18:57584325 | C | CA | 180 | a0001c0001t0001g0066 a0001c0001t0001g0116 a0001c0001t0003g0008 others(177): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.67+2228dupT | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584325 | |||||||
chr18:57584325 | C | CAA | 188 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(185): Show |
196 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(193): Show |
intron_variant | MODIFIER | c.67+2227_67+2228dup others(2): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584325 | |||||||
chr18:57584325 | C | CAAA | 16 | a0001c0001t0003g0079 a0001c0001t0006g0384 a0001c0001t0010g0382 others(13): Show |
16 | HG01109.hp1 HG01167.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+2226_67+2228dup others(3): Show |
FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584325 | |||||||
chr18:57584547 | G | A | 1 | a0003c0007t0084g0242 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67+2007C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584547 | |||||||
chr18:57584658 | G | A | 1 | a0002c0003t0001g0387 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67+1896C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584658 | |||||||
chr18:57584684 | G | A | 14 | a0001c0001t0001g0066 a0001c0001t0003g0008 a0001c0001t0003g0067 others(11): Show |
16 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(13): Show |
intron_variant | MODIFIER | c.67+1870C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584684 | |||||||
chr18:57584814 | T | C | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.67+1740A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584814 | |||||||
chr18:57584862 | G | A | 192 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(189): Show |
201 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(198): Show |
intron_variant | MODIFIER | c.67+1692C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57584862 | |||||||
chr18:57585074 | T | A | 2 | a0001c0001t0036g0243 a0001c0001t0037g0017 |
3 | NA18939.hp1 NA18980.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.67+1480A>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585074 | |||||||
chr18:57585122 | G | A | 1 | a0001c0001t0023g0388 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.67+1432C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585122 | |||||||
chr18:57585181 | C | T | 1 | a0001c0001t0108g0087 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67+1373G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585181 | |||||||
chr18:57585221 | A | C | 4 | a0001c0001t0015g0086 a0001c0001t0023g0085 a0001c0001t0039g0083 others(1): Show |
4 | HG01069.hp1 HG01167.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1333T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585221 | |||||||
chr18:57585381 | T | G | 154 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0263 others(151): Show |
158 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.67+1173A>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585381 | |||||||
chr18:57585411 | A | C | 4 | a0001c0002t0032g0003 a0001c0002t0032g0021 a0001c0002t0049g0022 others(1): Show |
5 | NA18943.hp2 NA18961.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1143T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585411 | |||||||
chr18:57585573 | A | G | 1 | a0001c0001t0216g0082 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.67+981T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585573 | |||||||
chr18:57585661 | G | A | 2 | a0001c0001t0028g0019 a0001c0001t0028g0389 |
3 | HG02922.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.67+893C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585661 | |||||||
chr18:57585671 | C | T | 1 | a0001c0001t0146g0081 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.67+883G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585671 | |||||||
chr18:57585755 | T | C | 11 | a0001c0001t0025g0394 a0001c0001t0029g0390 a0001c0001t0058g0395 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.67+799A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585755 | |||||||
chr18:57585871 | C | T | 1 | a0001c0001t0036g0080 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67+683G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57585871 | |||||||
chr18:57586067 | A | G | 1 | a0001c0001t0003g0079 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.67+487T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57586067 | |||||||
chr18:57586199 | A | G | 1 | a0001c0001t0024g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.67+355T>C | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57586199 | |||||||
chr18:57586253 | T | C | 1 | a0001c0001t0145g0401 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+301A>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57586253 | |||||||
chr18:57586421 | C | T | 1 | a0001c0002t0013g0077 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.67+133G>A | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57586421 | |||||||
chr18:57586457 | A | C | 3 | a0001c0002t0002g0074 a0001c0002t0002g0076 a0001c0002t0007g0075 |
3 | NA18975.hp1 NA19010.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.67+97T>G | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57586457 | |||||||
chr18:57586478 | G | A | 340 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0001c0001t0001g0255 others(337): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.67+76C>T | FECH | ENSG00000066926.13 | transcript | ENST00000262093.11 | protein_coding | 1/10 | chr18 | 57586478 |