geneid | 345757 |
---|---|
ensemblid | ENSG00000174132.9 |
hgncid | 24943 |
symbol | FAM174A |
name | family with sequence similarity 174 member A |
refseq_nuc | NM_198507.3 |
refseq_prot | NP_940909.1 |
ensembl_nuc | ENST00000312637.5 |
ensembl_prot | ENSP00000307954.2 |
mane_status | MANE Select |
chr | chr5 |
start | 100535374 |
end | 100586741 |
strand | + |
ver | v1.2 |
region | chr5:100535374-100586741 |
region5000 | chr5:100530374-100591741 |
regionname0 | FAM174A_chr5_100535374_100586741 |
regionname5000 | FAM174A_chr5_100530374_100591741 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 190 | 285 | 78 | 61 | 111 | 14 | 19 | 81 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0002 | 0/0 | 190 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0003 | 0/0 | 190 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0004 | 0/0 | 190 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0005 | 0/0 | 190 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 573 | 230 | 59 | 39 | 102 | 11 | 17 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
c0002 | 0/0 | 573 | 54 | 19 | 22 | 8 | 3 | 2 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
c0003 | 0/0 | 573 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
c0004 | 0/0 | 573 | 3 | 3 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
c0005 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
c0006 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
c0007 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 715 | 139 | 66 | 31 | 27 | 7 | 8 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0002 | 1/1 | 715 | 132 | 4 | 27 | 82 | 7 | 10 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0003 | 0/0 | 715 | 19 | 15 | 3 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0004 | 0/0 | 715 | 3 | 2 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0005 | 0/0 | 715 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0006 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0007 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
t0008 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0003 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0023 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 573 | 230 | 59 | 39 | 102 | 11 | 17 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0002 | 0/0 | 573 | 54 | 19 | 22 | 8 | 3 | 2 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0005 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0002c0003 | 0/0 | 573 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0003c0004 | 0/0 | 573 | 3 | 3 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0004c0007 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0005c0006 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1287 | 77 | 40 | 8 | 19 | 4 | 6 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0001t0002 | 1/1 | 1287 | 131 | 4 | 27 | 81 | 7 | 10 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0001t0003 | 0/0 | 1287 | 16 | 12 | 3 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0001t0004 | 0/0 | 1287 | 3 | 2 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0001t0005 | 0/0 | 1287 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0001t0007 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0002t0001 | 0/0 | 1287 | 53 | 19 | 22 | 8 | 3 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0002t0006 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0001c0005t0008 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0002c0003t0001 | 0/0 | 1287 | 8 | 7 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0003c0004t0003 | 0/0 | 1287 | 3 | 3 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0004c0007t0001 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
a0005c0006t0002 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | copy fasta | chr5 | 100530374 | 100591741 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0023 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0004g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0001c0005t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0002c0003t0001g0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0003c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0003c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0003c0004t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0004c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
a0005c0006t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0238 | EUR | GBR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0182 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00738 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0229 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0022 | EUR | IBS | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0065 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0233 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CDX | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0064 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0239 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02735 | hp2 | a0001 | c0002 | t0006 | g0237 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0224 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02895 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02897 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02965 | hp2 | a0003 | c0004 | t0003 | g0248 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02976 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03834 | hp1 | a0004 | c0007 | t0001 | g0003 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18964 | hp1 | a0005 | c0006 | t0002 | g0018 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18977 | hp1 | a0001 | c0005 | t0008 | g0250 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19030 | hp1 | a0003 | c0004 | t0003 | g0041 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0240 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ASW | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0183 | EUR | TSI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0230 | EUR | TSI | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | CLM | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | MSL | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0001 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA20300 | hp1 | a0003 | c0004 | t0003 | g0036 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | USA | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | LWK | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0023 | REF | REF | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0172 | REF | REF | FAM174A_chr5_100530374_100591741 | FAM174A | chr5 | 100530374 | 100591741 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:100535612
|
G | C | 1 | a0005 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.82G>C | p.Gly28Arg | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 239/1287 | 82/573 | 28/190 | chr5 | 100535612 | ||
chr5:100535655
|
G | A | 1 | a0004 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.125G>A | p.Gly42Asp | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 282/1287 | 125/573 | 42/190 | chr5 | 100535655 | ||
chr5:100535814
|
A | G | 1 | a0002 | 8 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
missense_variant | MODERATE | c.284A>G | p.Asp95Gly | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 441/1287 | 284/573 | 95/190 | chr5 | 100535814 | ||
chr5:100562176
|
A | G | 1 | a0003 | 3 | HG02965.hp2 NA19030.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.557A>G | p.Asn186Ser | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/3 | 714/1287 | 557/573 | 186/190 | chr5 | 100562176 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:100535602
|
T | C | 1 | a0001c0005 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.72T>C | p.Pro24Pro | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 229/1287 | 72/573 | 24/190 | chr5 | 100535602 | ||
chr5:100562162
|
G | A | 1 | a0001c0002 | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
synonymous_variant | LOW | c.543G>A | p.Thr181Thr | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/3 | 700/1287 | 543/573 | 181/190 | chr5 | 100562162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:100535393
|
T | A | 1 | a0001c0001t0004 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-138T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 138 | chr5 | 100535393 | |||||
chr5:100535437
|
C | G | 1 | a0001c0005t0008 | 1 | NA18977.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/3 | 94 | chr5 | 100535437 | |||||
chr5:100586373
|
C | T | 1 | a0001c0001t0007 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 189 | chr5 | 100586373 | |||||
chr5:100586377
|
G | A | 9 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*193G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 193 | chr5 | 100586377 | |||||
chr5:100586448
|
C | T | 1 | a0001c0001t0005 | 2 | HG00597.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*264C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 264 | chr5 | 100586448 | |||||
chr5:100586460
|
A | G | 2 | a0001c0001t0003a0003c0004t0003 | 19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*276A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 276 | chr5 | 100586460 | |||||
chr5:100586649
|
A | T | 1 | a0001c0002t0006 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 3/3 | 465 | chr5 | 100586649 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:100535992
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.434+28C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100535992 | ||||||
chr5:100536008
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.434+44C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536008 | ||||||
chr5:100536082
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.434+118T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536082 | ||||||
chr5:100536346
|
A | G | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.434+382A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536346 | ||||||
chr5:100536374
|
A | G | 3 | a0001c0001t0002g0251a0001c0001t0002g0252a0001c0001t0002g0253 | 3 | NA19057.hp1 NA19063.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.434+410A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536374 | ||||||
chr5:100536563
|
C | T | 1 | a0001c0005t0008g0250 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.434+599C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536563 | ||||||
chr5:100536650
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+686T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536650 | ||||||
chr5:100536748
|
G | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+784G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536748 | ||||||
chr5:100536765
|
C | T | 1 | a0003c0004t0003g0248 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434+801C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536765 | ||||||
chr5:100536820
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.434+856T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536820 | ||||||
chr5:100536890
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434+926A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100536890 | ||||||
chr5:100537355
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.434+1391C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537355 | ||||||
chr5:100537416
|
G | C | 13 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(10): Show | 15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.434+1452G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537416 | ||||||
chr5:100537545
|
A | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+1581A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537545 | ||||||
chr5:100537662
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.434+1698G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537662 | ||||||
chr5:100537750
|
A | G | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.434+1786A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537750 | ||||||
chr5:100537817
|
A | G | 36 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(33): Show | 45 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.434+1853A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537817 | ||||||
chr5:100537837
|
A | G | 46 | a0001c0001t0002g0216a0001c0002t0001g0002a0001c0002t0001g0026others(43): Show | 55 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.434+1873A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537837 | ||||||
chr5:100537933
|
A | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+1969A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100537933 | ||||||
chr5:100538045
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.434+2081T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538045 | ||||||
chr5:100538235
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.434+2271C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538235 | ||||||
chr5:100538337
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+2373G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538337 | ||||||
chr5:100538380
|
A | C | 1 | a0001c0001t0003g0206 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.434+2416A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538380 | ||||||
chr5:100538529
|
G | GTA | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0002t0001g0246 | 3 | HG00741.hp2 HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+2577_434+2578d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100538529 | |||||
chr5:100538554
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+2590G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538554 | ||||||
chr5:100538599
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.434+2635G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538599 | ||||||
chr5:100538657
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434+2693A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538657 | ||||||
chr5:100538717
|
A | G | 2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.434+2753A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538717 | ||||||
chr5:100538849
|
T | G | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.434+2885T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100538849 | ||||||
chr5:100539018
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.434+3054G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539018 | ||||||
chr5:100539028
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.434+3064C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539028 | ||||||
chr5:100539053
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+3089G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539053 | ||||||
chr5:100539075
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.434+3111T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539075 | ||||||
chr5:100539084
|
T | TTAAAAAA others(318): Show |
1 | a0003c0004t0003g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.434+3120_434+3121i others(327): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539084 | ||||||
chr5:100539085
|
A | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.434+3121A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539085 | ||||||
chr5:100539086
|
A | T | 31 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(28): Show | 39 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.434+3122A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539086 | ||||||
chr5:100539287
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.434+3323A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539287 | ||||||
chr5:100539370
|
T | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+3406T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539370 | ||||||
chr5:100539385
|
T | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.434+3421T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539385 | ||||||
chr5:100539566
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+3602G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539566 | ||||||
chr5:100539835
|
T | C | 5 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.434+3871T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539835 | ||||||
chr5:100539907
|
A | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+3943A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539907 | ||||||
chr5:100539948
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+3984G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539948 | ||||||
chr5:100539966
|
A | T | 1 | a0001c0001t0002g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.434+4002A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100539966 | ||||||
chr5:100540229
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.434+4265A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540229 | ||||||
chr5:100540338
|
T | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0206 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.434+4374T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540338 | ||||||
chr5:100540347
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434+4383T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540347 | ||||||
chr5:100540448
|
A | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+4484A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540448 | ||||||
chr5:100540498
|
T | G | 11 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0038others(8): Show | 13 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.434+4534T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540498 | ||||||
chr5:100540499
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.434+4535A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540499 | ||||||
chr5:100540553
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.434+4589A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540553 | ||||||
chr5:100540658
|
C | CT | 10 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0029others(7): Show | 13 | HG00140.hp2 HG01167.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.434+4695dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100540658 | |||||
chr5:100540899
|
G | A | 5 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0233others(2): Show | 7 | HG01167.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+4935G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100540899 | ||||||
chr5:100541011
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.434+5047A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541011 | ||||||
chr5:100541052
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0098 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.434+5088G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541052 | ||||||
chr5:100541160
|
A | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.434+5196A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541160 | ||||||
chr5:100541321
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.434+5357G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541321 | ||||||
chr5:100541630
|
A | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.434+5666A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541630 | ||||||
chr5:100541880
|
T | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+5916T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100541880 | ||||||
chr5:100542299
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+6335G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542299 | ||||||
chr5:100542328
|
T | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 200 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.434+6364T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542328 | ||||||
chr5:100542511
|
C | T | 1 | a0001c0002t0001g0232 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.434+6547C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542511 | ||||||
chr5:100542531
|
A | G | 1 | a0001c0001t0002g0025 | 2 | HG01934.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.434+6567A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542531 | ||||||
chr5:100542583
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.434+6619A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542583 | ||||||
chr5:100542621
|
A | G | 1 | a0001c0001t0002g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.434+6657A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542621 | ||||||
chr5:100542659
|
A | AC | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.434+6696dupC | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542659 | |||||
chr5:100542731
|
C | T | 10 | a0001c0001t0002g0046a0001c0001t0002g0192a0001c0001t0002g0193others(7): Show | 11 | HG00597.hp2 HG01928.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.434+6767C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542731 | ||||||
chr5:100542758
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+6794C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542758 | ||||||
chr5:100542846
|
A | ATATG | 7 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+6883_434+6884i others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | |||||
chr5:100542846
|
A | ATGTG | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+6898_434+6901d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | |||||
chr5:100542846
|
A | G | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.434+6882A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542846 | ||||||
chr5:100542846
|
ATG | A | 8 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0052others(5): Show | 13 | HG00738.hp1 HG00741.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.434+6900_434+6901d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | |||||
chr5:100542846
|
ATGTGTG | A | 4 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+6896_434+6901d others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100542846 | |||||
chr5:100542850
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0052 | 3 | HG00741.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434+6886G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542850 | ||||||
chr5:100542934
|
T | C | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.434+6970T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100542934 | ||||||
chr5:100543043
|
A | T | 1 | a0001c0002t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.434+7079A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543043 | ||||||
chr5:100543075
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.434+7111C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543075 | ||||||
chr5:100543079
|
G | A | 6 | a0001c0001t0002g0017a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 7 | NA18945.hp1 NA18948.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+7115G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543079 | ||||||
chr5:100543211
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434+7247G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543211 | ||||||
chr5:100543262
|
C | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7298C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543262 | ||||||
chr5:100543263
|
G | T | 51 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(48): Show | 60 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.434+7299G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543263 | ||||||
chr5:100543301
|
A | G | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.434+7337A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543301 | ||||||
chr5:100543436
|
G | A | 1 | a0001c0002t0001g0217 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.434+7472G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543436 | ||||||
chr5:100543550
|
C | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7586C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543550 | ||||||
chr5:100543676
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.434+7712A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543676 | ||||||
chr5:100543790
|
C | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7826C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543790 | ||||||
chr5:100543820
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+7856G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543820 | ||||||
chr5:100543952
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.434+7988G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543952 | ||||||
chr5:100543991
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0050others(8): Show | 12 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.434+8027A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100543991 | ||||||
chr5:100544036
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.434+8072G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544036 | ||||||
chr5:100544345
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+8381G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544345 | ||||||
chr5:100544348
|
ATACCCCT others(7): Show |
A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.434+8402_434+8415d others(16): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100544348 | |||||
chr5:100544427
|
G | C | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+8463G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544427 | ||||||
chr5:100544472
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+8508G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544472 | ||||||
chr5:100544949
|
C | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+8985C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544949 | ||||||
chr5:100544964
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434+9000T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100544964 | ||||||
chr5:100545067
|
A | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+9103A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545067 | ||||||
chr5:100545375
|
T | C | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+9411T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545375 | ||||||
chr5:100545378
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+9414G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545378 | ||||||
chr5:100545511
|
C | A | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.434+9547C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545511 | ||||||
chr5:100545557
|
G | T | 3 | a0002c0003t0001g0001a0002c0003t0001g0064a0002c0003t0001g0065 | 8 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+9593G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545557 | ||||||
chr5:100545682
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.434+9718A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545682 | ||||||
chr5:100545729
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.434+9765T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545729 | ||||||
chr5:100545904
|
T | C | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.434+9940T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545904 | ||||||
chr5:100545976
|
C | A | 1 | a0001c0001t0002g0019 | 2 | NA18941.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.434+10012C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100545976 | ||||||
chr5:100546009
|
T | C | 1 | a0001c0001t0002g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.434+10045T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546009 | ||||||
chr5:100546034
|
G | A | 4 | a0001c0001t0002g0046a0001c0001t0002g0192a0001c0001t0002g0193others(1): Show | 4 | HG04228.hp1 NA18612.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.434+10070G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546034 | ||||||
chr5:100546071
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.434+10107A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546071 | ||||||
chr5:100546437
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+10473G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546437 | ||||||
chr5:100546715
|
C | T | 80 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 96 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.434+10751C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546715 | ||||||
chr5:100546730
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+10766A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546730 | ||||||
chr5:100546792
|
C | T | 13 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(10): Show | 15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.434+10828C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100546792 | ||||||
chr5:100547603
|
T | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.434+11639T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547603 | ||||||
chr5:100547648
|
C | T | 7 | a0001c0002t0001g0002a0001c0002t0001g0226a0001c0002t0001g0227others(4): Show | 11 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.434+11684C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547648 | ||||||
chr5:100547667
|
G | A | 34 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(31): Show | 42 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.434+11703G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547667 | ||||||
chr5:100547677
|
T | C | 8 | a0001c0001t0003g0006a0001c0001t0003g0038a0001c0001t0003g0039others(5): Show | 9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.434+11713T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547677 | ||||||
chr5:100547752
|
G | T | 2 | a0001c0001t0002g0187a0001c0001t0002g0188 | 2 | HG00408.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.434+11788G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547752 | ||||||
chr5:100547833
|
TA | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+11870delA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547833 | ||||||
chr5:100547834
|
A | AT | 5 | a0001c0001t0002g0046a0001c0001t0004g0030a0001c0001t0004g0249others(2): Show | 6 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+11880dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100547834 | |||||
chr5:100547834
|
A | T | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+11870A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547834 | ||||||
chr5:100547873
|
G | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 55 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.434+11909G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547873 | ||||||
chr5:100547928
|
C | T | 1 | a0001c0001t0002g0131 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.434+11964C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100547928 | ||||||
chr5:100548025
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+12061A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548025 | ||||||
chr5:100548054
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+12090T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548054 | ||||||
chr5:100548604
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.434+12640G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548604 | ||||||
chr5:100548612
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.434+12648G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100548612 | ||||||
chr5:100548921
|
TCA | T | 6 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.434+12959_434+1296 others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100548921 | |||||
chr5:100549167
|
G | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-12887G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549167 | ||||||
chr5:100549188
|
G | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-12866G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549188 | ||||||
chr5:100549261
|
A | G | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.435-12793A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549261 | ||||||
chr5:100549478
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.435-12576T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549478 | ||||||
chr5:100549607
|
AT | A | 6 | a0001c0002t0001g0217a0001c0002t0001g0239a0001c0002t0001g0240others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-12431delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100549607 | |||||
chr5:100549821
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-12233C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549821 | ||||||
chr5:100549932
|
T | G | 1 | a0001c0002t0001g0236 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.435-12122T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100549932 | ||||||
chr5:100550043
|
A | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-12011A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550043 | ||||||
chr5:100550067
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.435-11987G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550067 | ||||||
chr5:100550384
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0085a0001c0001t0001g0086 | 4 | HG01433.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-11670C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550384 | ||||||
chr5:100550710
|
G | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-11344G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550710 | ||||||
chr5:100550842
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.435-11212A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100550842 | ||||||
chr5:100551315
|
A | G | 1 | a0001c0001t0005g0024 | 2 | HG00597.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.435-10739A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551315 | ||||||
chr5:100551377
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.435-10677C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551377 | ||||||
chr5:100551399
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.435-10655C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551399 | ||||||
chr5:100551817
|
G | A | 1 | a0001c0001t0002g0020 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.435-10237G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551817 | ||||||
chr5:100551897
|
A | G | 1 | a0001c0001t0001g0013 | 2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.435-10157A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100551897 | ||||||
chr5:100552128
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.435-9926G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552128 | ||||||
chr5:100552309
|
T | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-9745T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552309 | ||||||
chr5:100552451
|
A | T | 1 | a0001c0001t0002g0130 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.435-9603A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552451 | ||||||
chr5:100552491
|
G | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-9563G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552491 | ||||||
chr5:100552982
|
A | G | 1 | a0001c0002t0001g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.435-9072A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100552982 | ||||||
chr5:100553034
|
T | G | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-9020T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553034 | ||||||
chr5:100553055
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.435-8999T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553055 | ||||||
chr5:100553138
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.435-8916A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553138 | ||||||
chr5:100553143
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.435-8911C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553143 | ||||||
chr5:100553223
|
A | T | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.435-8831A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553223 | ||||||
chr5:100553374
|
T | C | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-8680T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553374 | ||||||
chr5:100553397
|
A | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-8657A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553397 | ||||||
chr5:100553722
|
A | G | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-8332A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553722 | ||||||
chr5:100553954
|
G | C | 1 | a0001c0001t0002g0135 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.435-8100G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100553954 | ||||||
chr5:100554009
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.435-8045C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554009 | ||||||
chr5:100554276
|
C | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7778C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554276 | ||||||
chr5:100554304
|
TTCTA | T | 5 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211others(2): Show | 5 | HG01243.hp1 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-7746_435-7743d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554304 | |||||
chr5:100554310
|
C | CT | 9 | a0001c0001t0002g0133a0001c0001t0002g0183a0001c0001t0003g0040others(6): Show | 10 | HG01109.hp2 HG02451.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.435-7721dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554310 | |||||
chr5:100554310
|
CT | C | 88 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0050others(85): Show | 101 | HG00140.hp2 HG00621.hp2 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.435-7721delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554310 | |||||
chr5:100554310
|
CTT | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 67 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.435-7722_435-7721d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554310 | |||||
chr5:100554363
|
C | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7691C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554363 | ||||||
chr5:100554387
|
G | A | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-7667G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554387 | ||||||
chr5:100554447
|
G | A | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-7607G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554447 | ||||||
chr5:100554462
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-7592G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554462 | ||||||
chr5:100554604
|
C | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7450C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554604 | ||||||
chr5:100554643
|
A | G | 1 | a0001c0001t0002g0135 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.435-7411A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554643 | ||||||
chr5:100554643
|
AT | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 96 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.435-7408delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100554643 | |||||
chr5:100554868
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0138a0001c0001t0002g0190 | 4 | HG00140.hp1 HG01071.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-7186G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554868 | ||||||
chr5:100554882
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.435-7172A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554882 | ||||||
chr5:100554904
|
T | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0108a0001c0001t0002g0109others(1): Show | 4 | NA18964.hp1 NA18970.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-7150T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554904 | ||||||
chr5:100554910
|
T | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-7144T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554910 | ||||||
chr5:100554923
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-7131G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554923 | ||||||
chr5:100554947
|
C | T | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-7107C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554947 | ||||||
chr5:100554957
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.435-7097T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100554957 | ||||||
chr5:100555041
|
T | C | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-7013T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555041 | ||||||
chr5:100555069
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0090others(5): Show | 9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.435-6985C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555069 | ||||||
chr5:100555077
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.435-6977C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555077 | ||||||
chr5:100555092
|
C | A | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435-6962C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555092 | ||||||
chr5:100555103
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.435-6951G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555103 | ||||||
chr5:100555156
|
G | C | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-6898G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555156 | ||||||
chr5:100555197
|
C | T | 17 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(14): Show | 19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.435-6857C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555197 | ||||||
chr5:100555209
|
G | C | 47 | a0001c0001t0004g0030a0001c0001t0004g0249a0001c0002t0001g0002others(44): Show | 57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-6845G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555209 | ||||||
chr5:100555244
|
C | G | 1 | a0001c0001t0002g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.435-6810C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555244 | ||||||
chr5:100555274
|
G | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-6780G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555274 | ||||||
chr5:100555433
|
G | C | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.435-6621G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555433 | ||||||
chr5:100555449
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.435-6605C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555449 | ||||||
chr5:100555498
|
C | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-6556C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555498 | ||||||
chr5:100555499
|
G | A | 2 | a0001c0001t0002g0138a0001c0002t0001g0218 | 2 | HG03942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.435-6555G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555499 | ||||||
chr5:100555526
|
C | G | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-6528C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555526 | ||||||
chr5:100555538
|
C | G | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-6516C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555538 | ||||||
chr5:100555582
|
T | C | 50 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247others(47): Show | 61 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.435-6472T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555582 | ||||||
chr5:100555614
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-6440C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555614 | ||||||
chr5:100555656
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.435-6398G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555656 | ||||||
chr5:100555707
|
G | A | 1 | a0001c0001t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.435-6347G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555707 | ||||||
chr5:100555778
|
G | GT | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-6269dupT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100555778 | |||||
chr5:100555800
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.435-6254T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555800 | ||||||
chr5:100555809
|
T | C | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-6245T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555809 | ||||||
chr5:100555821
|
C | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-6233C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555821 | ||||||
chr5:100555888
|
A | C | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-6166A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555888 | ||||||
chr5:100555897
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.435-6157G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555897 | ||||||
chr5:100555930
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.435-6124G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100555930 | ||||||
chr5:100555941
|
GT | G | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-6110delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100555941 | |||||
chr5:100556000
|
G | A | 4 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-6054G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556000 | ||||||
chr5:100556022
|
C | T | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-6032C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556022 | ||||||
chr5:100556065
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.435-5989T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556065 | ||||||
chr5:100556151
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.435-5903C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556151 | ||||||
chr5:100556161
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.435-5893G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556161 | ||||||
chr5:100556303
|
C | G | 2 | a0001c0001t0001g0128a0001c0001t0002g0127 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.435-5751C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556303 | ||||||
chr5:100556391
|
C | T | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-5663C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556391 | ||||||
chr5:100556493
|
C | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-5561C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556493 | ||||||
chr5:100556543
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 99 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.435-5511T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556543 | ||||||
chr5:100556549
|
C | T | 37 | a0001c0001t0001g0128a0001c0001t0002g0017a0001c0001t0002g0018others(34): Show | 38 | HG00621.hp2 HG01099.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.435-5505C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556549 | ||||||
chr5:100556650
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(130): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-5404T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556650 | ||||||
chr5:100556672
|
A | G | 2 | a0001c0001t0003g0056a0001c0001t0003g0206 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.435-5382A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556672 | ||||||
chr5:100556702
|
C | G | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-5352C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556702 | ||||||
chr5:100556724
|
C | G | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.435-5330C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556724 | ||||||
chr5:100556740
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0042a0001c0001t0003g0044 | 4 | HG01167.hp1 HG01169.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-5314G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556740 | ||||||
chr5:100556956
|
C | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-5098C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100556956 | ||||||
chr5:100557121
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.435-4933G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557121 | ||||||
chr5:100557201
|
C | A | 13 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(10): Show | 15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.435-4853C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557201 | ||||||
chr5:100557220
|
G | A | 6 | a0001c0001t0002g0136a0001c0001t0002g0141a0001c0001t0002g0142others(3): Show | 6 | HG02056.hp1 HG02074.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.435-4834G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557220 | ||||||
chr5:100557220
|
G | GTTCTGTT | 50 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247others(47): Show | 61 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.435-4833_435-4832i others(9): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 100557220 | |||||
chr5:100557223
|
C | T | 50 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247others(47): Show | 61 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.435-4831C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557223 | ||||||
chr5:100557273
|
G | A | 46 | a0001c0001t0001g0069a0001c0002t0001g0002a0001c0002t0001g0026others(43): Show | 55 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.435-4781G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557273 | ||||||
chr5:100557288
|
A | G | 1 | a0001c0001t0002g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.435-4766A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557288 | ||||||
chr5:100557513
|
A | G | 3 | a0001c0001t0004g0030a0001c0001t0004g0249a0001c0002t0001g0224 | 4 | HG01109.hp2 HG02451.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-4541A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557513 | ||||||
chr5:100557544
|
C | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.435-4510C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557544 | ||||||
chr5:100557588
|
G | T | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-4466G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557588 | ||||||
chr5:100557593
|
T | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0050others(8): Show | 12 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.435-4461T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557593 | ||||||
chr5:100557605
|
C | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 63 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.435-4449C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557605 | ||||||
chr5:100557627
|
T | G | 3 | a0002c0003t0001g0001a0002c0003t0001g0064a0002c0003t0001g0065 | 8 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.435-4427T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557627 | ||||||
chr5:100557677
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-4377T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557677 | ||||||
chr5:100557851
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-4203G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557851 | ||||||
chr5:100557927
|
C | G | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-4127C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100557927 | ||||||
chr5:100558032
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-4022C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558032 | ||||||
chr5:100558033
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.435-4021G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558033 | ||||||
chr5:100558046
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.435-4008A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558046 | ||||||
chr5:100558203
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.435-3851G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558203 | ||||||
chr5:100558233
|
T | C | 1 | a0001c0001t0003g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.435-3821T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558233 | ||||||
chr5:100558293
|
G | T | 1 | a0001c0001t0002g0126 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.435-3761G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558293 | ||||||
chr5:100558343
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.435-3711G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558343 | ||||||
chr5:100558428
|
G | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG02809.hp2 HG02818.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-3626G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558428 | ||||||
chr5:100558478
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.435-3576G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558478 | ||||||
chr5:100558563
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.435-3491G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558563 | ||||||
chr5:100558763
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435-3291C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558763 | ||||||
chr5:100558795
|
T | C | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.435-3259T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558795 | ||||||
chr5:100558935
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.435-3119A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558935 | ||||||
chr5:100558955
|
G | T | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.435-3099G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100558955 | ||||||
chr5:100559128
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG02559.hp1 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.435-2926G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559128 | ||||||
chr5:100559172
|
T | G | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2882T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559172 | ||||||
chr5:100559190
|
T | C | 47 | a0001c0001t0004g0030a0001c0001t0004g0249a0001c0002t0001g0002others(44): Show | 57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-2864T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559190 | ||||||
chr5:100559193
|
A | T | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-2861A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559193 | ||||||
chr5:100559223
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.435-2831C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559223 | ||||||
chr5:100559242
|
C | A | 1 | a0001c0002t0001g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435-2812C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559242 | ||||||
chr5:100559297
|
C | T | 1 | a0001c0002t0001g0217 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.435-2757C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559297 | ||||||
chr5:100559328
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.435-2726C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559328 | ||||||
chr5:100559344
|
G | A | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2710G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559344 | ||||||
chr5:100559496
|
A | G | 1 | a0001c0002t0001g0230 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.435-2558A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559496 | ||||||
chr5:100559643
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0042a0001c0001t0003g0044 | 4 | HG01167.hp1 HG01169.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-2411G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559643 | ||||||
chr5:100559839
|
A | T | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.435-2215A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559839 | ||||||
chr5:100559840
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-2214G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559840 | ||||||
chr5:100559846
|
T | A | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2208T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559846 | ||||||
chr5:100559846
|
T | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0044 | 3 | HG01167.hp1 HG01169.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.435-2208T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559846 | ||||||
chr5:100559928
|
G | A | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.435-2126G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100559928 | ||||||
chr5:100560208
|
G | A | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.435-1846G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560208 | ||||||
chr5:100560256
|
A | C | 1 | a0001c0001t0002g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.435-1798A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560256 | ||||||
chr5:100560267
|
A | T | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.435-1787A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560267 | ||||||
chr5:100560414
|
C | T | 83 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 99 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.435-1640C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560414 | ||||||
chr5:100560490
|
T | C | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.435-1564T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560490 | ||||||
chr5:100560540
|
A | G | 47 | a0001c0001t0004g0030a0001c0001t0004g0249a0001c0002t0001g0002others(44): Show | 57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-1514A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560540 | ||||||
chr5:100560557
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-1497T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560557 | ||||||
chr5:100560730
|
T | G | 1 | a0001c0001t0003g0043 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.435-1324T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560730 | ||||||
chr5:100560864
|
C | G | 47 | a0001c0001t0004g0030a0001c0001t0004g0249a0001c0002t0001g0002others(44): Show | 57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.435-1190C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560864 | ||||||
chr5:100560920
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.435-1134A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560920 | ||||||
chr5:100560948
|
C | G | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-1106C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100560948 | ||||||
chr5:100561067
|
G | T | 1 | a0001c0001t0003g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.435-987G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561067 | ||||||
chr5:100561471
|
T | C | 3 | a0001c0001t0002g0127a0001c0001t0002g0147a0001c0001t0002g0148 | 3 | HG00741.hp1 HG01255.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.435-583T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561471 | ||||||
chr5:100561524
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.435-530T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561524 | ||||||
chr5:100561634
|
A | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-420A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561634 | ||||||
chr5:100561639
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.435-415C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561639 | ||||||
chr5:100561681
|
C | T | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.435-373C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561681 | ||||||
chr5:100561682
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.435-372G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561682 | ||||||
chr5:100561768
|
C | T | 7 | a0001c0001t0002g0105a0001c0001t0002g0107a0001c0001t0002g0120others(4): Show | 7 | HG02015.hp1 HG02040.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.435-286C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561768 | ||||||
chr5:100561769
|
G | A | 1 | a0001c0002t0006g0237 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.435-285G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | chr5 | 100561769 | ||||||
chr5:100562451
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.569+263G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562451 | ||||||
chr5:100562468
|
T | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0129 | 2 | HG02027.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.569+280T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562468 | ||||||
chr5:100562474
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.569+286A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562474 | ||||||
chr5:100562509
|
T | G | 1 | a0001c0001t0002g0146 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.569+321T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562509 | ||||||
chr5:100562631
|
T | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+443T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562631 | ||||||
chr5:100562633
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.569+445A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562633 | ||||||
chr5:100562701
|
T | C | 11 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0038others(8): Show | 13 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.569+513T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562701 | ||||||
chr5:100562984
|
G | A | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+796G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562984 | ||||||
chr5:100562985
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+797C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100562985 | ||||||
chr5:100563147
|
T | C | 54 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(51): Show | 63 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.569+959T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563147 | ||||||
chr5:100563179
|
A | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+991A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563179 | ||||||
chr5:100563250
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.569+1062C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563250 | ||||||
chr5:100563282
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.569+1094A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563282 | ||||||
chr5:100563315
|
A | T | 1 | a0001c0001t0001g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.569+1127A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563315 | ||||||
chr5:100563339
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.569+1151C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563339 | ||||||
chr5:100563372
|
AT | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+1188delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100563372 | |||||
chr5:100563400
|
C | CA | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+1224dupA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100563400 | |||||
chr5:100563400
|
CA | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 98 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.569+1224delA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100563400 | |||||
chr5:100563476
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.569+1288G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563476 | ||||||
chr5:100563614
|
G | C | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG01243.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.569+1426G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563614 | ||||||
chr5:100563667
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.569+1479C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563667 | ||||||
chr5:100563763
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.569+1575T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563763 | ||||||
chr5:100563986
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.569+1798G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100563986 | ||||||
chr5:100564054
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.569+1866C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564054 | ||||||
chr5:100564072
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(127): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.569+1884G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564072 | ||||||
chr5:100564183
|
G | A | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.569+1995G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564183 | ||||||
chr5:100564310
|
A | G | 47 | a0001c0001t0004g0030a0001c0001t0004g0249a0001c0002t0001g0002others(44): Show | 57 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.569+2122A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564310 | ||||||
chr5:100564336
|
C | CA | 31 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0003g0056others(28): Show | 39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.569+2158dupA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100564336 | |||||
chr5:100564337
|
A | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569+2149A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564337 | ||||||
chr5:100564350
|
C | A | 1 | a0001c0001t0002g0151 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.569+2162C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564350 | ||||||
chr5:100564364
|
T | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0001g0247 | 4 | HG02486.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+2176T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564364 | ||||||
chr5:100564604
|
C | T | 17 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(14): Show | 19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.569+2416C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564604 | ||||||
chr5:100564695
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.569+2507A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564695 | ||||||
chr5:100564700
|
C | T | 45 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(42): Show | 54 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.569+2512C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564700 | ||||||
chr5:100564755
|
C | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+2567C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564755 | ||||||
chr5:100564917
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.569+2729G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100564917 | ||||||
chr5:100565094
|
T | TA | 64 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(61): Show | 76 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(73): Show |
intron_variant | MODIFIER | c.569+2906_569+2907i others(3): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565094 | ||||||
chr5:100565113
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.569+2925A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565113 | ||||||
chr5:100565168
|
A | C | 8 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.569+2980A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565168 | ||||||
chr5:100565518
|
A | G | 37 | a0001c0001t0001g0128a0001c0001t0002g0017a0001c0001t0002g0018others(34): Show | 38 | HG00621.hp2 HG01099.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.569+3330A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565518 | ||||||
chr5:100565607
|
A | G | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+3419A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565607 | ||||||
chr5:100565613
|
T | G | 1 | a0001c0001t0002g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.569+3425T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565613 | ||||||
chr5:100565760
|
T | A | 1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.569+3572T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565760 | ||||||
chr5:100565763
|
G | A | 1 | a0001c0002t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.569+3575G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565763 | ||||||
chr5:100565827
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.569+3639G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565827 | ||||||
chr5:100565925
|
T | C | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.569+3737T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100565925 | ||||||
chr5:100566004
|
C | CTT | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+3817_569+3818d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566004 | |||||
chr5:100566141
|
G | GAT | 22 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0061others(19): Show | 30 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.569+3982_569+3983d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAGATA others(1): Show |
2 | a0001c0002t0001g0026a0001c0002t0001g0231 | 3 | HG01071.hp2 HG01123.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.569+3956_569+3957i others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAGATA others(5): Show |
2 | a0001c0002t0001g0224a0001c0002t0001g0234 | 2 | HG01167.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.569+3956_569+3957i others(14): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAGATA others(7): Show |
4 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0229others(1): Show | 6 | HG01516.hp2 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+3956_569+3957i others(16): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAGATA others(9): Show |
5 | a0001c0002t0001g0027a0001c0002t0001g0218a0001c0002t0001g0227others(2): Show | 6 | HG01081.hp2 HG01192.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+3956_569+3957i others(18): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAGATA others(11): Show |
5 | a0001c0002t0001g0002a0001c0002t0001g0219a0001c0002t0001g0230others(2): Show | 9 | HG00140.hp2 HG00735.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+3956_569+3957i others(20): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAGATA others(13): Show |
3 | a0001c0002t0001g0217a0001c0002t0001g0226a0001c0002t0006g0237 | 3 | HG02293.hp2 HG02735.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.569+3956_569+3957i others(22): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATAT | 27 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0054others(24): Show | 29 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.569+3980_569+3983d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATAT | 33 | a0001c0001t0001g0035a0001c0001t0001g0068a0001c0001t0001g0072others(30): Show | 34 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.569+3978_569+3983d others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATATA others(1): Show |
33 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(30): Show | 37 | HG00408.hp1 HG01099.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.569+3976_569+3983d others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATATA others(3): Show |
26 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0070others(23): Show | 28 | HG00621.hp1 HG01358.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.569+3974_569+3983d others(12): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATATA others(5): Show |
29 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0016others(26): Show | 32 | HG00323.hp2 HG00597.hp1 HG02135.hp1 others(29): Show |
intron_variant | MODIFIER | c.569+3972_569+3983d others(14): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATATA others(7): Show |
22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 28 | HG00099.hp2 HG00280.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.569+3970_569+3983d others(16): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATATA others(9): Show |
4 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0086others(1): Show | 4 | HG00621.hp2 HG02015.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+3968_569+3983d others(18): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
G | GATATATA others(13): Show |
2 | a0001c0001t0002g0111a0001c0001t0002g0253 | 2 | NA19004.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.569+3964_569+3983d others(22): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
GAT | G | 5 | a0001c0001t0002g0125a0001c0001t0002g0127a0001c0001t0002g0174others(2): Show | 5 | HG00642.hp1 HG01243.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+3982_569+3983d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
GATAT | G | 6 | a0001c0001t0002g0023a0001c0001t0002g0025a0001c0001t0002g0123others(3): Show | 8 | HG01934.hp1 HG02015.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.569+3980_569+3983d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
GATATATA others(1): Show |
G | 3 | a0001c0001t0002g0124a0001c0001t0003g0037a0001c0001t0003g0045 | 3 | HG02056.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.569+3976_569+3983d others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566141
|
GATATATA others(3): Show |
G | 17 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0038others(14): Show | 20 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.569+3974_569+3983d others(12): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566141 | |||||
chr5:100566145
|
T | G | 2 | a0001c0001t0002g0179a0001c0001t0002g0244 | 2 | HG01243.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.569+3957T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566145 | ||||||
chr5:100566210
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569+4022T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566210 | ||||||
chr5:100566249
|
A | T | 2 | a0001c0001t0002g0151a0001c0001t0002g0173 | 2 | HG00438.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.569+4061A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566249 | ||||||
chr5:100566271
|
A | G | 3 | a0001c0001t0001g0093a0001c0002t0001g0254a0001c0002t0001g0255 | 3 | HG01891.hp2 HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.569+4083A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566271 | ||||||
chr5:100566307
|
TAGAA | T | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0080others(5): Show | 13 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.569+4123_569+4126d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100566307 | |||||
chr5:100566479
|
G | A | 4 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+4291G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566479 | ||||||
chr5:100566500
|
G | T | 4 | a0001c0002t0001g0027a0001c0002t0001g0028a0001c0002t0001g0233others(1): Show | 6 | HG01934.hp2 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+4312G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566500 | ||||||
chr5:100566712
|
G | A | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.569+4524G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566712 | ||||||
chr5:100566745
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.569+4557C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566745 | ||||||
chr5:100566828
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.569+4640T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100566828 | ||||||
chr5:100567289
|
CAAAT | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0002g0245others(1): Show | 6 | HG02486.hp1 HG02922.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+5102_569+5105d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567289 | ||||||
chr5:100567367
|
C | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.569+5179C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567367 | ||||||
chr5:100567404
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.569+5216A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567404 | ||||||
chr5:100567723
|
GT | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(83): Show | 108 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.569+5538delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100567723 | |||||
chr5:100567855
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.569+5667C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567855 | ||||||
chr5:100567974
|
A | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+5786A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100567974 | ||||||
chr5:100568024
|
G | T | 1 | a0001c0001t0002g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.569+5836G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568024 | ||||||
chr5:100568198
|
A | G | 13 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(10): Show | 15 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.569+6010A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568198 | ||||||
chr5:100568202
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | NA18960.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.569+6014C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568202 | ||||||
chr5:100568260
|
A | T | 8 | a0001c0001t0003g0006a0001c0001t0003g0038a0001c0001t0003g0039others(5): Show | 9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+6072A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568260 | ||||||
chr5:100568536
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+6348C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568536 | ||||||
chr5:100568592
|
T | TTTGTTTT others(17): Show |
2 | a0001c0001t0002g0022a0001c0001t0002g0191 | 3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6406_569+6407i others(26): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100568592 | |||||
chr5:100568597
|
A | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0191 | 3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6409A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568597 | ||||||
chr5:100568599
|
A | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0191 | 3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6411A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568599 | ||||||
chr5:100568601
|
T | TTTTGCC | 2 | a0001c0001t0002g0022a0001c0001t0002g0191 | 3 | HG00738.hp2 HG01358.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.569+6414_569+6415i others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100568601 | |||||
chr5:100568737
|
A | AG | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+6549_569+6550i others(3): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568737 | ||||||
chr5:100568752
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0002g0245 | 4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+6564G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568752 | ||||||
chr5:100568789
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0002g0173 | 2 | HG00438.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.569+6601A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568789 | ||||||
chr5:100568800
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.569+6612G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568800 | ||||||
chr5:100568828
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+6640G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568828 | ||||||
chr5:100568830
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0095 | 3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+6642T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568830 | ||||||
chr5:100568916
|
A | AGGTTTCT others(5): Show |
19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+6729_569+6740d others(14): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100568916 | |||||
chr5:100568969
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.569+6781A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568969 | ||||||
chr5:100568987
|
A | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+6799A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100568987 | ||||||
chr5:100569065
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0002g0245 | 4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+6877T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569065 | ||||||
chr5:100569311
|
A | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02717.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.569+7123A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569311 | ||||||
chr5:100569348
|
C | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+7160C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569348 | ||||||
chr5:100569352
|
T | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+7164T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569352 | ||||||
chr5:100569387
|
A | T | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.569+7199A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569387 | ||||||
chr5:100569391
|
T | TTA | 88 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0034others(85): Show | 106 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(103): Show |
intron_variant | MODIFIER | c.569+7215_569+7216d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100569391 | |||||
chr5:100569391
|
T | TTATA | 49 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 58 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.569+7213_569+7216d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100569391 | |||||
chr5:100569525
|
A | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0084 | 2 | HG01358.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.569+7337A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569525 | ||||||
chr5:100569530
|
C | T | 6 | a0001c0002t0001g0208a0001c0002t0001g0209a0001c0002t0001g0210others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+7342C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569530 | ||||||
chr5:100569532
|
C | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+7344C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569532 | ||||||
chr5:100569663
|
T | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0066 | 3 | HG00099.hp2 HG01192.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.569+7475T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569663 | ||||||
chr5:100569732
|
G | C | 1 | a0001c0001t0002g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.569+7544G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569732 | ||||||
chr5:100569733
|
G | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+7545G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569733 | ||||||
chr5:100569837
|
G | GAT | 3 | a0001c0001t0002g0190a0001c0002t0001g0239a0001c0002t0001g0243 | 3 | HG02683.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.569+7664_569+7665d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100569837 | |||||
chr5:100569854
|
C | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0054 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.569+7666C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569854 | ||||||
chr5:100569925
|
G | A | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+7737G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100569925 | ||||||
chr5:100570330
|
A | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+8142A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570330 | ||||||
chr5:100570518
|
A | C | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+8330A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570518 | ||||||
chr5:100570559
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.569+8371G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570559 | ||||||
chr5:100570675
|
G | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+8487G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570675 | ||||||
chr5:100570690
|
A | G | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+8502A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570690 | ||||||
chr5:100570809
|
A | G | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.569+8621A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570809 | ||||||
chr5:100570833
|
G | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0095 | 3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+8645G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100570833 | ||||||
chr5:100571143
|
TA | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+8956delA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571143 | ||||||
chr5:100571152
|
G | GTA | 97 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.569+8974_569+8975d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571152 | |||||
chr5:100571164
|
G | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.569+8976G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571164 | ||||||
chr5:100571262
|
G | A | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.569+9074G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571262 | ||||||
chr5:100571334
|
G | C | 1 | a0001c0001t0001g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.569+9146G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571334 | ||||||
chr5:100571365
|
A | T | 4 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+9177A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571365 | ||||||
chr5:100571386
|
G | C | 1 | a0001c0001t0002g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.569+9198G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571386 | ||||||
chr5:100571444
|
T | C | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.569+9256T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571444 | ||||||
chr5:100571446
|
G | T | 8 | a0001c0001t0003g0006a0001c0001t0003g0038a0001c0001t0003g0039others(5): Show | 9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.569+9258G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571446 | ||||||
chr5:100571469
|
A | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0002g0245 | 4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+9281A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571469 | ||||||
chr5:100571496
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.569+9308G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571496 | ||||||
chr5:100571661
|
A | AGT | 5 | a0001c0001t0002g0179a0001c0001t0003g0056a0001c0001t0003g0062others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+9484_569+9485d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571661 | |||||
chr5:100571672
|
G | A | 6 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 6 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.569+9484G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571672 | ||||||
chr5:100571672
|
G | GTA | 63 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 80 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.569+9503_569+9504d others(4): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | |||||
chr5:100571672
|
G | GTATA | 14 | a0001c0001t0001g0034a0001c0001t0001g0057a0001c0001t0001g0058others(11): Show | 15 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.569+9501_569+9504d others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | |||||
chr5:100571672
|
G | GTATATA | 26 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0002t0001g0002others(23): Show | 32 | HG00140.hp2 HG00735.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.569+9499_569+9504d others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | |||||
chr5:100571672
|
G | GTATATAT others(1): Show |
9 | a0001c0001t0001g0048a0001c0002t0001g0026a0001c0002t0001g0029others(6): Show | 12 | HG01071.hp2 HG01256.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.569+9497_569+9504d others(10): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | |||||
chr5:100571672
|
G | GTGTATAT others(3): Show |
2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.569+9485_569+9486i others(12): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | |||||
chr5:100571672
|
G | GTGTGTA | 10 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0002t0001g0208others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.569+9485_569+9486i others(8): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100571672 | |||||
chr5:100571691
|
T | C | 3 | a0001c0001t0002g0201a0001c0002t0001g0254a0001c0002t0001g0255 | 3 | HG01258.hp2 HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.569+9503T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571691 | ||||||
chr5:100571693
|
C | T | 73 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(70): Show | 90 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.569+9505C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571693 | ||||||
chr5:100571695
|
C | T | 2 | a0001c0001t0003g0062a0001c0001t0003g0063 | 2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.569+9507C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571695 | ||||||
chr5:100571754
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.569+9566T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571754 | ||||||
chr5:100571828
|
C | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+9640C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571828 | ||||||
chr5:100571969
|
T | C | 1 | a0001c0001t0002g0019 | 2 | NA18941.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.569+9781T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100571969 | ||||||
chr5:100572171
|
G | C | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+9983G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572171 | ||||||
chr5:100572206
|
T | G | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+10018T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572206 | ||||||
chr5:100572215
|
CT | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.569+10035delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100572215 | |||||
chr5:100572233
|
CT | C | 30 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0058others(27): Show | 31 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.569+10057delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100572233 | |||||
chr5:100572247
|
C | A | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.569+10059C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572247 | ||||||
chr5:100572250
|
CT | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 11 | HG02486.hp1 HG02559.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.569+10074delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100572250 | |||||
chr5:100572399
|
G | A | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+10211G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572399 | ||||||
chr5:100572403
|
C | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+10215C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572403 | ||||||
chr5:100572472
|
G | A | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+10284G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572472 | ||||||
chr5:100572498
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.569+10310G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572498 | ||||||
chr5:100572504
|
C | T | 4 | a0001c0001t0001g0128a0002c0003t0001g0001a0002c0003t0001g0064others(1): Show | 9 | HG00738.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.569+10316C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572504 | ||||||
chr5:100572520
|
C | T | 10 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0002t0001g0208others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.569+10332C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572520 | ||||||
chr5:100572521
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.569+10333G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572521 | ||||||
chr5:100572597
|
C | G | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.569+10409C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572597 | ||||||
chr5:100572619
|
A | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+10431A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572619 | ||||||
chr5:100572722
|
G | A | 9 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0063others(6): Show | 11 | HG01167.hp2 HG01884.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.569+10534G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572722 | ||||||
chr5:100572893
|
C | G | 1 | a0001c0001t0002g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.569+10705C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100572893 | ||||||
chr5:100573059
|
AGT | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.569+10874_569+1087 others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100573059 | |||||
chr5:100573076
|
T | C | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569+10888T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573076 | ||||||
chr5:100573129
|
T | G | 2 | a0001c0001t0002g0153a0001c0001t0002g0161 | 2 | NA18945.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.569+10941T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573129 | ||||||
chr5:100573138
|
G | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.569+10950G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573138 | ||||||
chr5:100573153
|
C | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0095 | 3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+10965C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573153 | ||||||
chr5:100573161
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0161 | 2 | NA18945.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.569+10973C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573161 | ||||||
chr5:100573196
|
G | T | 2 | a0001c0002t0001g0254a0001c0002t0001g0255 | 2 | HG01891.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.569+11008G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573196 | ||||||
chr5:100573255
|
A | C | 1 | a0002c0003t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.569+11067A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573255 | ||||||
chr5:100573334
|
A | G | 17 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(14): Show | 19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.569+11146A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573334 | ||||||
chr5:100573379
|
GT | G | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.569+11195delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100573379 | |||||
chr5:100573388
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0095 | 3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.569+11200C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573388 | ||||||
chr5:100573425
|
T | C | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.569+11237T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573425 | ||||||
chr5:100573691
|
T | C | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.569+11503T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573691 | ||||||
chr5:100573712
|
C | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.569+11524C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573712 | ||||||
chr5:100573737
|
T | C | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.569+11549T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573737 | ||||||
chr5:100573742
|
A | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+11554A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573742 | ||||||
chr5:100573760
|
A | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | HG02809.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+11572A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573760 | ||||||
chr5:100573864
|
G | T | 4 | a0001c0001t0003g0056a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | HG01884.hp2 HG02257.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.569+11676G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573864 | ||||||
chr5:100573894
|
C | T | 5 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | HG01123.hp1 HG02300.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+11706C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573894 | ||||||
chr5:100573921
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.569+11733G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100573921 | ||||||
chr5:100574190
|
AT | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.570-11983delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100574190 | |||||
chr5:100574215
|
A | C | 3 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0184 | 3 | HG00280.hp1 HG01106.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.570-11966A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574215 | ||||||
chr5:100574326
|
T | C | 1 | a0001c0001t0002g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570-11855T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574326 | ||||||
chr5:100574562
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(131): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.570-11619G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574562 | ||||||
chr5:100574584
|
A | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-11597A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574584 | ||||||
chr5:100574667
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.570-11514T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574667 | ||||||
chr5:100574717
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.570-11464G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574717 | ||||||
chr5:100574882
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570-11299C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574882 | ||||||
chr5:100574911
|
C | G | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-11270C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100574911 | ||||||
chr5:100575022
|
T | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(135): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.570-11159T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575022 | ||||||
chr5:100575119
|
T | C | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-11062T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575119 | ||||||
chr5:100575217
|
C | T | 19 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(16): Show | 22 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.570-10964C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575217 | ||||||
chr5:100575246
|
T | TTA | 4 | a0001c0001t0002g0120a0001c0001t0002g0123a0001c0001t0002g0168others(1): Show | 4 | HG01255.hp2 HG02015.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.570-10921_570-1092 others(6): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100575246 | |||||
chr5:100575368
|
A | T | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.570-10813A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575368 | ||||||
chr5:100575397
|
G | A | 8 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(5): Show | 8 | HG02647.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.570-10784G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575397 | ||||||
chr5:100575441
|
T | C | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-10740T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575441 | ||||||
chr5:100575506
|
G | A | 2 | a0001c0001t0002g0114a0001c0001t0002g0117 | 2 | NA18971.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.570-10675G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575506 | ||||||
chr5:100575539
|
A | G | 1 | a0001c0002t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570-10642A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575539 | ||||||
chr5:100575572
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.570-10609A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575572 | ||||||
chr5:100575605
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.570-10576A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575605 | ||||||
chr5:100575659
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.570-10522G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575659 | ||||||
chr5:100575784
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0095a0001c0001t0002g0245 | 4 | HG02486.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-10397A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575784 | ||||||
chr5:100575803
|
T | C | 1 | a0001c0001t0002g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.570-10378T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575803 | ||||||
chr5:100575932
|
G | A | 11 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0038others(8): Show | 13 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.570-10249G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100575932 | ||||||
chr5:100576120
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0090others(5): Show | 9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-10061C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576120 | ||||||
chr5:100576151
|
C | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(43): Show | 55 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.570-10030C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576151 | ||||||
chr5:100576346
|
C | T | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-9835C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576346 | ||||||
chr5:100576356
|
C | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-9825C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576356 | ||||||
chr5:100576379
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0002g0189 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.570-9802T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576379 | ||||||
chr5:100576554
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.570-9627G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576554 | ||||||
chr5:100576702
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.570-9479A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576702 | ||||||
chr5:100576738
|
A | G | 4 | a0001c0002t0001g0239a0001c0002t0001g0243a0001c0002t0001g0254others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.570-9443A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576738 | ||||||
chr5:100576791
|
A | T | 1 | a0001c0001t0002g0121 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.570-9390A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100576791 | ||||||
chr5:100577253
|
A | C | 1 | a0001c0001t0002g0139 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.570-8928A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577253 | ||||||
chr5:100577391
|
G | T | 1 | a0001c0001t0002g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.570-8790G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577391 | ||||||
chr5:100577499
|
A | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.570-8682A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577499 | ||||||
chr5:100577552
|
C | T | 6 | a0001c0001t0002g0017a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 7 | NA18945.hp1 NA18948.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-8629C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577552 | ||||||
chr5:100577570
|
C | A | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-8611C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577570 | ||||||
chr5:100577787
|
A | G | 1 | a0001c0001t0002g0156 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.570-8394A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577787 | ||||||
chr5:100577857
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-8324T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577857 | ||||||
chr5:100577916
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.570-8265G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577916 | ||||||
chr5:100577951
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.570-8230T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100577951 | ||||||
chr5:100578017
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0249 | 3 | HG01109.hp2 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.570-8164G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578017 | ||||||
chr5:100578153
|
G | C | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.570-8028G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578153 | ||||||
chr5:100578188
|
A | G | 2 | a0001c0001t0002g0146a0001c0001t0002g0176 | 2 | NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.570-7993A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578188 | ||||||
chr5:100578319
|
G | A | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.570-7862G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578319 | ||||||
chr5:100578443
|
T | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-7738T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578443 | ||||||
chr5:100578462
|
G | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-7719G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578462 | ||||||
chr5:100578530
|
C | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-7651C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100578530 | ||||||
chr5:100579032
|
A | G | 6 | a0001c0001t0002g0017a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 7 | NA18945.hp1 NA18948.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.570-7149A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579032 | ||||||
chr5:100579092
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.570-7089T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579092 | ||||||
chr5:100579171
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.570-7010A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579171 | ||||||
chr5:100579633
|
T | C | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-6548T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579633 | ||||||
chr5:100579757
|
A | T | 1 | a0001c0001t0002g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.570-6424A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100579757 | ||||||
chr5:100580029
|
C | T | 8 | a0001c0001t0003g0006a0001c0001t0003g0038a0001c0001t0003g0039others(5): Show | 9 | HG01109.hp1 HG02647.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.570-6152C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580029 | ||||||
chr5:100580168
|
A | T | 1 | a0001c0001t0002g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.570-6013A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580168 | ||||||
chr5:100580188
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0090others(5): Show | 9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-5993G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580188 | ||||||
chr5:100580189
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.570-5992C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580189 | ||||||
chr5:100580234
|
A | G | 2 | a0001c0002t0001g0031a0001c0002t0001g0256 | 3 | HG02486.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.570-5947A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580234 | ||||||
chr5:100580261
|
G | GA | 27 | a0001c0002t0001g0002a0001c0002t0001g0026a0001c0002t0001g0027others(24): Show | 35 | HG00140.hp2 HG00735.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.570-5915dupA | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100580261 | |||||
chr5:100580268
|
G | A | 2 | a0001c0001t0001g0247a0001c0002t0001g0246 | 2 | HG01255.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.570-5913G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580268 | ||||||
chr5:100580571
|
A | T | 1 | a0001c0001t0001g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.570-5610A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580571 | ||||||
chr5:100580588
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.570-5593G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580588 | ||||||
chr5:100580648
|
C | G | 1 | a0001c0001t0002g0126 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.570-5533C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580648 | ||||||
chr5:100580762
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.570-5419T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580762 | ||||||
chr5:100580849
|
G | A | 1 | a0001c0001t0002g0171 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.570-5332G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580849 | ||||||
chr5:100580950
|
T | G | 1 | a0001c0001t0004g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.570-5231T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580950 | ||||||
chr5:100580980
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0090others(5): Show | 9 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-5201C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100580980 | ||||||
chr5:100581004
|
C | G | 1 | a0001c0001t0002g0108 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.570-5177C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581004 | ||||||
chr5:100581030
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0207 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.570-5151G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581030 | ||||||
chr5:100581032
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.570-5149G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581032 | ||||||
chr5:100581100
|
C | G | 20 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(17): Show | 23 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.570-5081C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581100 | ||||||
chr5:100581323
|
A | G | 1 | a0001c0001t0003g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.570-4858A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581323 | ||||||
chr5:100581409
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.570-4772G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581409 | ||||||
chr5:100581556
|
C | T | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4625C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581556 | ||||||
chr5:100581557
|
T | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4624T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581557 | ||||||
chr5:100581558
|
C | G | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4623C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581558 | ||||||
chr5:100581559
|
G | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4622G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581559 | ||||||
chr5:100581560
|
C | A | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4621C>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581560 | ||||||
chr5:100581562
|
T | TC | 26 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.570-4619_570-4618i others(3): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581562 | ||||||
chr5:100581578
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.570-4603T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581578 | ||||||
chr5:100581891
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0095 | 3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.570-4290T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100581891 | ||||||
chr5:100582350
|
A | G | 1 | a0003c0004t0003g0041 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.570-3831A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582350 | ||||||
chr5:100582462
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0048others(6): Show | 9 | HG00741.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.570-3719T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582462 | ||||||
chr5:100582474
|
GT | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(9): Show | 14 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.570-3696delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100582474 | |||||
chr5:100582515
|
C | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(42): Show | 49 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.570-3666C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582515 | ||||||
chr5:100582897
|
C | T | 2 | a0001c0002t0001g0214a0001c0002t0001g0215 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.570-3284C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100582897 | ||||||
chr5:100583541
|
C | T | 1 | a0001c0001t0003g0006 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.570-2640C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583541 | ||||||
chr5:100583549
|
T | A | 17 | a0001c0001t0003g0006a0001c0001t0003g0007a0001c0001t0003g0037others(14): Show | 19 | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.570-2632T>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583549 | ||||||
chr5:100583638
|
AT | A | 15 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(12): Show | 15 | HG00408.hp2 HG01167.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.570-2531delT | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 100583638 | |||||
chr5:100583795
|
A | G | 36 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0001t0001g0247others(33): Show | 40 | HG01109.hp1 HG01109.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.570-2386A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583795 | ||||||
chr5:100583799
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.570-2382G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100583799 | ||||||
chr5:100584244
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.570-1937C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584244 | ||||||
chr5:100584246
|
C | G | 10 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0002t0001g0208others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.570-1935C>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584246 | ||||||
chr5:100584322
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(134): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.570-1859T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584322 | ||||||
chr5:100584338
|
G | C | 1 | a0001c0001t0003g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.570-1843G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584338 | ||||||
chr5:100584585
|
T | G | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.570-1596T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584585 | ||||||
chr5:100584601
|
G | T | 17 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0001t0001g0247others(14): Show | 18 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.570-1580G>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584601 | ||||||
chr5:100584680
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.570-1501A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584680 | ||||||
chr5:100584813
|
T | C | 1 | a0001c0002t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.570-1368T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584813 | ||||||
chr5:100584832
|
C | T | 97 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.570-1349C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584832 | ||||||
chr5:100584965
|
A | G | 1 | a0001c0002t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.570-1216A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100584965 | ||||||
chr5:100585242
|
A | G | 1 | a0001c0001t0002g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.570-939A>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585242 | ||||||
chr5:100585266
|
C | T | 1 | a0001c0001t0002g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570-915C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585266 | ||||||
chr5:100585301
|
T | C | 18 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0001t0001g0247others(15): Show | 19 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.570-880T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585301 | ||||||
chr5:100585487
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.570-694A>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585487 | ||||||
chr5:100585506
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.570-675C>T | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585506 | ||||||
chr5:100585563
|
G | A | 10 | a0001c0001t0001g0166a0001c0001t0001g0200a0001c0002t0001g0208others(7): Show | 10 | HG01243.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.570-618G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585563 | ||||||
chr5:100585710
|
G | A | 1 | a0001c0001t0007g0089 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.570-471G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585710 | ||||||
chr5:100585731
|
A | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0043 | 2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.570-450A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585731 | ||||||
chr5:100585781
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.570-400A>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585781 | ||||||
chr5:100585855
|
G | A | 1 | a0001c0002t0001g0225 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.570-326G>A | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585855 | ||||||
chr5:100585878
|
T | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0095 | 3 | HG02486.hp1 HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.570-303T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100585878 | ||||||
chr5:100586004
|
T | G | 1 | a0001c0001t0003g0040 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.570-177T>G | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100586004 | ||||||
chr5:100586120
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00741.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570-61T>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100586120 | ||||||
chr5:100586137
|
G | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(133): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.570-44G>C | FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 2/2 | chr5 | 100586137 |