geneid | 84103 |
---|---|
ensemblid | ENSG00000138813.10 |
hgncid | 25274 |
symbol | C4orf17 |
name | chromosome 4 open reading frame 17 |
refseq_nuc | NM_032149.3 |
refseq_prot | NP_115525.2 |
ensembl_nuc | ENST00000326581.9 |
ensembl_prot | ENSP00000322582.4 |
mane_status | MANE Select |
chr | chr4 |
start | 99511021 |
end | 99542303 |
strand | + |
ver | v1.2 |
region | chr4:99511021-99542303 |
region5000 | chr4:99506021-99547303 |
regionname0 | C4orf17_chr4_99511021_99542303 |
regionname5000 | C4orf17_chr4_99506021_99547303 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 359 | 177 | 9 | 46 | 106 | 5 | 9 | 89 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002 | 0/0 | 359 | 86 | 37 | 8 | 33 | 0 | 8 | 30 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0003 | 0/0 | 359 | 75 | 22 | 12 | 25 | 1 | 15 | 22 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0004 | 0/0 | 359 | 29 | 11 | 5 | 8 | 0 | 5 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0005 | 0/0 | 355 | 18 | 17 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0006 | 0/0 | 359 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1080 | 176 | 9 | 46 | 106 | 5 | 9 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0002 | 0/0 | 1080 | 72 | 19 | 12 | 25 | 1 | 15 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0003 | 0/0 | 1080 | 43 | 9 | 1 | 32 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0004 | 0/0 | 1080 | 36 | 21 | 7 | 1 | 0 | 7 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0005 | 0/0 | 1080 | 29 | 11 | 5 | 8 | 0 | 5 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0006 | 0/0 | 1068 | 18 | 17 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0007 | 0/0 | 1080 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0008 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0009 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0010 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
c0011 | 0/1 | 1080 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 540 | 386 | 96 | 72 | 172 | 6 | 38 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0016 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1080 | 176 | 9 | 46 | 106 | 5 | 9 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0001c0011 | 0/1 | 1080 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0003 | 0/0 | 1080 | 43 | 9 | 1 | 32 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0004 | 0/0 | 1080 | 36 | 21 | 7 | 1 | 0 | 7 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0007 | 0/0 | 1080 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0009 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0003c0002 | 0/0 | 1080 | 72 | 19 | 12 | 25 | 1 | 15 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0003c0008 | 0/0 | 1080 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0004c0005 | 0/0 | 1080 | 29 | 11 | 5 | 8 | 0 | 5 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0005c0006 | 0/0 | 1068 | 18 | 17 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0006c0010 | 0/0 | 1080 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1619 | 176 | 9 | 46 | 106 | 5 | 9 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0001c0011t0001 | 0/1 | 1619 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0003t0001 | 0/0 | 1619 | 43 | 9 | 1 | 32 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0004t0001 | 0/0 | 1619 | 36 | 21 | 7 | 1 | 0 | 7 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0007t0001 | 0/0 | 1619 | 4 | 4 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0002c0009t0001 | 0/0 | 1619 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0003c0002t0001 | 0/0 | 1619 | 72 | 19 | 12 | 25 | 1 | 15 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0003c0008t0001 | 0/0 | 1619 | 3 | 3 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0004c0005t0001 | 0/0 | 1619 | 29 | 11 | 5 | 8 | 0 | 5 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0005c0006t0001 | 0/0 | 1607 | 18 | 17 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
a0006c0010t0001 | 0/0 | 1619 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | copy fasta | chr4 | 99506021 | 99547303 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0001c0011t0001g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0004t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0007t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0007t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0007t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0007t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0009t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0002c0009t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0008t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0003c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0004c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0005c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
a0006c0010t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0002 | t0001 | g0205 | EUR | GBR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00438 | hp2 | a0004 | c0005 | t0001 | g0054 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00544 | hp1 | a0004 | c0005 | t0001 | g0051 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00558 | hp1 | a0004 | c0005 | t0001 | g0009 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00558 | hp2 | a0002 | c0003 | t0001 | g0292 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0302 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00639 | hp2 | a0002 | c0004 | t0001 | g0035 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00733 | hp1 | a0004 | c0005 | t0001 | g0048 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00741 | hp1 | a0003 | c0002 | t0001 | g0067 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01070 | hp1 | a0002 | c0004 | t0001 | g0027 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01070 | hp2 | a0002 | c0003 | t0001 | g0315 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0027 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01074 | hp1 | a0002 | c0004 | t0001 | g0247 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01106 | hp1 | a0003 | c0002 | t0001 | g0223 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01106 | hp2 | a0003 | c0002 | t0001 | g0180 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01109 | hp1 | a0004 | c0005 | t0001 | g0039 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01167 | hp1 | a0003 | c0002 | t0001 | g0225 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01167 | hp2 | a0003 | c0002 | t0001 | g0213 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01168 | hp2 | a0004 | c0005 | t0001 | g0036 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01169 | hp2 | a0003 | c0002 | t0001 | g0224 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01192 | hp1 | a0003 | c0002 | t0001 | g0218 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01192 | hp2 | a0004 | c0005 | t0001 | g0041 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01243 | hp1 | a0002 | c0004 | t0001 | g0032 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01243 | hp2 | a0004 | c0005 | t0001 | g0045 | AMR | PUR | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01255 | hp2 | a0003 | c0002 | t0001 | g0221 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0034 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01361 | hp1 | a0003 | c0002 | t0001 | g0181 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01361 | hp2 | a0002 | c0004 | t0001 | g0033 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01884 | hp1 | a0003 | c0002 | t0001 | g0203 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01884 | hp2 | a0005 | c0006 | t0001 | g0273 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01891 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01934 | hp1 | a0003 | c0002 | t0001 | g0194 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01975 | hp2 | a0005 | c0006 | t0001 | g0272 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02015 | hp1 | a0003 | c0002 | t0001 | g0214 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02027 | hp2 | a0003 | c0002 | t0001 | g0206 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02040 | hp1 | a0003 | c0002 | t0001 | g0022 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02055 | hp1 | a0004 | c0005 | t0001 | g0040 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02055 | hp2 | a0003 | c0002 | t0001 | g0193 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02056 | hp2 | a0004 | c0005 | t0001 | g0052 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02071 | hp2 | a0004 | c0005 | t0001 | g0009 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02083 | hp1 | a0004 | c0005 | t0001 | g0047 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02132 | hp2 | a0004 | c0005 | t0001 | g0056 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02145 | hp2 | a0002 | c0007 | t0001 | g0307 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02148 | hp1 | a0003 | c0002 | t0001 | g0178 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02257 | hp2 | a0002 | c0004 | t0001 | g0325 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02258 | hp1 | a0005 | c0006 | t0001 | g0029 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02258 | hp2 | a0003 | c0002 | t0001 | g0066 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02280 | hp1 | a0002 | c0004 | t0001 | g0063 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02280 | hp2 | a0002 | c0004 | t0001 | g0252 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02451 | hp1 | a0003 | c0002 | t0001 | g0207 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02451 | hp2 | a0004 | c0005 | t0001 | g0246 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02602 | hp1 | a0003 | c0002 | t0001 | g0220 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02602 | hp2 | a0004 | c0005 | t0001 | g0049 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02615 | hp1 | a0005 | c0006 | t0001 | g0269 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02615 | hp2 | a0003 | c0008 | t0001 | g0091 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02622 | hp1 | a0003 | c0002 | t0001 | g0227 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02622 | hp2 | a0005 | c0006 | t0001 | g0270 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02630 | hp1 | a0002 | c0004 | t0001 | g0248 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02630 | hp2 | a0002 | c0004 | t0001 | g0264 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02647 | hp1 | a0002 | c0009 | t0001 | g0101 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02698 | hp2 | a0003 | c0002 | t0001 | g0200 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02717 | hp1 | a0003 | c0002 | t0001 | g0211 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02723 | hp2 | a0002 | c0009 | t0001 | g0102 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02735 | hp1 | a0002 | c0004 | t0001 | g0259 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02735 | hp2 | a0003 | c0002 | t0001 | g0327 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02738 | hp1 | a0003 | c0002 | t0001 | g0226 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02738 | hp2 | a0003 | c0002 | t0001 | g0186 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02809 | hp1 | a0002 | c0003 | t0001 | g0305 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02809 | hp2 | a0005 | c0006 | t0001 | g0029 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02818 | hp1 | a0002 | c0004 | t0001 | g0267 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02818 | hp2 | a0003 | c0002 | t0001 | g0182 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02886 | hp1 | a0003 | c0002 | t0001 | g0201 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02886 | hp2 | a0004 | c0005 | t0001 | g0038 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02895 | hp2 | a0003 | c0002 | t0001 | g0171 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02896 | hp1 | a0002 | c0004 | t0001 | g0062 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02896 | hp2 | a0002 | c0004 | t0001 | g0028 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02897 | hp1 | a0002 | c0004 | t0001 | g0263 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02897 | hp2 | a0003 | c0002 | t0001 | g0170 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02922 | hp1 | a0005 | c0006 | t0001 | g0278 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02922 | hp2 | a0002 | c0004 | t0001 | g0104 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02965 | hp1 | a0005 | c0006 | t0001 | g0279 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02965 | hp2 | a0004 | c0005 | t0001 | g0046 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02970 | hp1 | a0003 | c0002 | t0001 | g0197 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02970 | hp2 | a0002 | c0009 | t0001 | g0286 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02976 | hp1 | a0003 | c0002 | t0001 | g0199 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02976 | hp2 | a0002 | c0007 | t0001 | g0323 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03017 | hp1 | a0003 | c0002 | t0001 | g0216 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03017 | hp2 | a0003 | c0002 | t0001 | g0219 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03041 | hp1 | a0005 | c0006 | t0001 | g0030 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03041 | hp2 | a0002 | c0003 | t0001 | g0304 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03098 | hp1 | a0003 | c0002 | t0001 | g0282 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03098 | hp2 | a0002 | c0004 | t0001 | g0243 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03130 | hp1 | a0002 | c0004 | t0001 | g0028 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03130 | hp2 | a0005 | c0006 | t0001 | g0030 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03139 | hp1 | a0003 | c0008 | t0001 | g0093 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03139 | hp2 | a0004 | c0005 | t0001 | g0037 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03195 | hp1 | a0002 | c0004 | t0001 | g0173 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03195 | hp2 | a0002 | c0007 | t0001 | g0320 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0318 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03225 | hp2 | a0002 | c0004 | t0001 | g0254 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03453 | hp1 | a0005 | c0006 | t0001 | g0277 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03453 | hp2 | a0002 | c0004 | t0001 | g0265 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03486 | hp1 | a0002 | c0007 | t0001 | g0296 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03486 | hp2 | a0005 | c0006 | t0001 | g0061 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03490 | hp2 | a0003 | c0002 | t0001 | g0050 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03491 | hp1 | a0002 | c0004 | t0001 | g0256 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03492 | hp1 | a0002 | c0004 | t0001 | g0255 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03516 | hp1 | a0005 | c0006 | t0001 | g0281 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03516 | hp2 | a0002 | c0004 | t0001 | g0262 | AFR | ESN | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03540 | hp1 | a0003 | c0002 | t0001 | g0202 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03540 | hp2 | a0004 | c0005 | t0001 | g0042 | AFR | GWD | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03579 | hp1 | a0002 | c0003 | t0001 | g0324 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03579 | hp2 | a0003 | c0002 | t0001 | g0105 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03654 | hp1 | a0003 | c0002 | t0001 | g0175 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03669 | hp1 | a0003 | c0002 | t0001 | g0212 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03669 | hp2 | a0002 | c0004 | t0001 | g0284 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03688 | hp1 | a0003 | c0002 | t0001 | g0176 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03688 | hp2 | a0002 | c0004 | t0001 | g0258 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03704 | hp2 | a0002 | c0004 | t0001 | g0260 | SAS | PJL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03834 | hp1 | a0004 | c0005 | t0001 | g0058 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03834 | hp2 | a0006 | c0010 | t0001 | g0242 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03927 | hp2 | a0003 | c0002 | t0001 | g0228 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03942 | hp1 | a0003 | c0002 | t0001 | g0192 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03942 | hp2 | a0004 | c0005 | t0001 | g0059 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG04115 | hp2 | a0003 | c0002 | t0001 | g0179 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG04184 | hp2 | a0003 | c0002 | t0001 | g0185 | SAS | BEB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG04228 | hp1 | a0002 | c0004 | t0001 | g0266 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG04228 | hp2 | a0002 | c0003 | t0001 | g0290 | SAS | STU | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18906 | hp1 | a0003 | c0002 | t0001 | g0196 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18906 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18940 | hp2 | a0002 | c0003 | t0001 | g0295 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0322 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18944 | hp1 | a0003 | c0002 | t0001 | g0217 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18946 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18947 | hp1 | a0004 | c0005 | t0001 | g0057 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18947 | hp2 | a0002 | c0003 | t0001 | g0316 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18948 | hp1 | a0003 | c0002 | t0001 | g0198 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18949 | hp1 | a0002 | c0003 | t0001 | g0291 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18956 | hp1 | a0002 | c0003 | t0001 | g0317 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18956 | hp2 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18959 | hp1 | a0003 | c0002 | t0001 | g0190 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18960 | hp1 | a0003 | c0002 | t0001 | g0215 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18960 | hp2 | a0002 | c0003 | t0001 | g0293 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18961 | hp1 | a0003 | c0002 | t0001 | g0172 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18965 | hp1 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18965 | hp2 | a0003 | c0002 | t0001 | g0060 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18967 | hp2 | a0003 | c0002 | t0001 | g0222 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18969 | hp1 | a0003 | c0002 | t0001 | g0022 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18972 | hp1 | a0002 | c0003 | t0001 | g0289 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18975 | hp2 | a0003 | c0002 | t0001 | g0191 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18976 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18976 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18978 | hp1 | a0002 | c0003 | t0001 | g0314 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18979 | hp2 | a0003 | c0002 | t0001 | g0195 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18986 | hp1 | a0002 | c0003 | t0001 | g0301 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18987 | hp1 | a0002 | c0004 | t0001 | g0261 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18987 | hp2 | a0002 | c0003 | t0001 | g0297 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18991 | hp1 | a0003 | c0002 | t0001 | g0210 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18993 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18994 | hp2 | a0003 | c0002 | t0001 | g0183 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19003 | hp1 | a0003 | c0002 | t0001 | g0023 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19004 | hp2 | a0002 | c0003 | t0001 | g0299 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19010 | hp1 | a0003 | c0002 | t0001 | g0023 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19012 | hp1 | a0003 | c0002 | t0001 | g0006 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19030 | hp1 | a0002 | c0004 | t0001 | g0251 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19030 | hp2 | a0005 | c0006 | t0001 | g0271 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0095 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19054 | hp2 | a0002 | c0003 | t0001 | g0294 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19058 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19060 | hp1 | a0003 | c0002 | t0001 | g0209 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19062 | hp1 | a0003 | c0002 | t0001 | g0204 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19065 | hp2 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0298 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19077 | hp2 | a0003 | c0002 | t0001 | g0187 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19080 | hp1 | a0003 | c0002 | t0001 | g0188 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19081 | hp2 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19083 | hp2 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19087 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19089 | hp2 | a0002 | c0003 | t0001 | g0321 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19090 | hp1 | a0003 | c0002 | t0001 | g0184 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19240 | hp1 | a0004 | c0005 | t0001 | g0043 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA19240 | hp2 | a0005 | c0006 | t0001 | g0274 | AFR | YRI | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA20129 | hp1 | a0002 | c0003 | t0001 | g0308 | AFR | ASW | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA20129 | hp2 | a0005 | c0006 | t0001 | g0280 | AFR | ASW | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA20905 | hp1 | a0004 | c0005 | t0001 | g0055 | SAS | GIH | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA20905 | hp2 | a0004 | c0005 | t0001 | g0053 | SAS | GIH | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG01123 | hp2 | a0003 | c0002 | t0001 | g0208 | AMR | CLM | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02109 | hp1 | a0002 | c0004 | t0001 | g0268 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02109 | hp2 | a0002 | c0003 | t0001 | g0312 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02486 | hp1 | a0005 | c0006 | t0001 | g0276 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02486 | hp2 | a0004 | c0005 | t0001 | g0244 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02559 | hp1 | a0003 | c0002 | t0001 | g0106 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG02559 | hp2 | a0005 | c0006 | t0001 | g0275 | AFR | ACB | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03471 | hp1 | a0002 | c0004 | t0001 | g0249 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG03471 | hp2 | a0003 | c0002 | t0001 | g0107 | AFR | MSL | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0253 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
HG06807 | hp2 | a0003 | c0008 | t0001 | g0092 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA20300 | hp1 | a0003 | c0002 | t0001 | g0189 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0319 | AFR | USA | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0257 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
NA21309 | hp2 | a0004 | c0005 | t0001 | g0044 | AFR | LWK | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
homoSapiens_chm13v2 | hp1 | a0001 | c0011 | t0001 | g0016 | REF | REF | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | C4orf17_chr4_99506021_99547303 | C4orf17 | chr4 | 99506021 | 99547303 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99522563
|
G | A | 2 | a0003a0004 | 104 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(101): Show |
missense_variant | MODERATE | c.191G>A | p.Gly64Glu | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 536/1619 | 191/1080 | 64/359 | chr4 | 99522563 | ||
chr4:99522625
|
T | C | 5 | a0002a0003a0004others(2): Show | 209 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(206): Show |
missense_variant | MODERATE | c.253T>C | p.Ser85Pro | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 598/1619 | 253/1080 | 85/359 | chr4 | 99522625 | ||
chr4:99522643
|
G | A | 1 | a0003 | 75 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(72): Show |
missense_variant | MODERATE | c.271G>A | p.Glu91Lys | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 616/1619 | 271/1080 | 91/359 | chr4 | 99522643 | ||
chr4:99529881
|
TCAGGGAT others(5): Show |
T | 1 | a0005 | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
disruptive_inframe_deletion | MODERATE | c.470_481delCAGGGATG others(4): Show |
p.Ser157_Ser161delin others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/9 | 815/1619 | 470/1080 | 157/359 | chr4 | 99529881 | ||
chr4:99529894
|
G | A | 1 | a0005 | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
missense_variant | MODERATE | c.482G>A | p.Ser161Asn | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/9 | 827/1619 | 482/1080 | 161/359 | chr4 | 99529894 | ||
chr4:99542101
|
C | T | 1 | a0006 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1072C>T | p.Arg358Trp | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 9/9 | 1417/1619 | 1072/1080 | 358/359 | chr4 | 99542101 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99522627
|
C | G | 2 | a0002c0009a0003c0002 | 75 | HG00140.hp1 HG00741.hp1 HG01106.hp1 others(72): Show |
synonymous_variant | LOW | c.255C>G | p.Ser85Ser | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 600/1619 | 255/1080 | 85/359 | chr4 | 99522627 | ||
chr4:99522696
|
A | G | 3 | a0002c0003a0002c0007a0002c0009 | 50 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(47): Show |
synonymous_variant | LOW | c.324A>G | p.Pro108Pro | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/9 | 669/1619 | 324/1080 | 108/359 | chr4 | 99522696 | ||
chr4:99537683
|
C | G | 1 | a0001c0011 | 1 | homoSapiens_chm13v2.hp1 | synonymous_variant | LOW | c.561C>G | p.Leu187Leu | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/9 | 906/1619 | 561/1080 | 187/359 | chr4 | 99537683 | ||
chr4:99539356
|
G | A | 1 | a0002c0007 | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.822G>A | p.Gly274Gly | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/9 | 1167/1619 | 822/1080 | 274/359 | chr4 | 99539356 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99511423
|
C | CT | 45 | a0001c0001t0001g0285a0001c0001t0001g0326a0002c0003t0001g0007others(42): Show | 48 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-94+162dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99511423 | |||||
chr4:99511423
|
CT | C | 30 | a0002c0004t0001g0062a0002c0004t0001g0063a0003c0002t0001g0050others(27): Show | 32 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.-94+162delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99511423 | |||||
chr4:99511426
|
T | C | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+154T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511426 | ||||||
chr4:99511555
|
C | G | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-94+283C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511555 | ||||||
chr4:99511684
|
G | A | 43 | a0001c0001t0001g0285a0002c0003t0001g0007a0002c0003t0001g0031others(40): Show | 46 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.-94+412G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511684 | ||||||
chr4:99511703
|
A | G | 1 | a0002c0004t0001g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-94+431A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511703 | ||||||
chr4:99511866
|
T | C | 2 | a0003c0002t0001g0066a0003c0002t0001g0067 | 2 | HG00741.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-94+594T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511866 | ||||||
chr4:99511887
|
A | C | 1 | a0001c0001t0001g0283 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-94+615A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511887 | ||||||
chr4:99511972
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(28): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-94+700G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511972 | ||||||
chr4:99511990
|
C | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0094a0002c0003t0001g0095others(3): Show | 7 | HG00735.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-94+718C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99511990 | ||||||
chr4:99512139
|
A | T | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-850A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512139 | ||||||
chr4:99512195
|
C | T | 19 | a0002c0004t0001g0062a0002c0004t0001g0063a0003c0002t0001g0282others(16): Show | 21 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93-794C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512195 | ||||||
chr4:99512196
|
G | A | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-93-793G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512196 | ||||||
chr4:99512327
|
G | A | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-662G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512327 | ||||||
chr4:99512345
|
G | C | 1 | a0002c0004t0001g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-93-644G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512345 | ||||||
chr4:99512352
|
C | T | 25 | a0001c0001t0001g0250a0002c0004t0001g0028a0002c0004t0001g0247others(22): Show | 26 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-93-637C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512352 | ||||||
chr4:99512380
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-93-609C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512380 | ||||||
chr4:99512451
|
C | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01261.hp2 HG01358.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93-538C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512451 | ||||||
chr4:99512579
|
A | C | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93-410A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512579 | ||||||
chr4:99512638
|
GTCA | G | 24 | a0001c0001t0001g0250a0002c0004t0001g0028a0002c0004t0001g0247others(21): Show | 25 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93-346_-93-344del others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99512638 | |||||
chr4:99512812
|
T | A | 1 | a0002c0004t0001g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-93-177T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512812 | ||||||
chr4:99512870
|
C | A | 1 | a0001c0001t0001g0285 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-93-119C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512870 | ||||||
chr4:99512904
|
C | T | 1 | a0004c0005t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-93-85C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 1/8 | chr4 | 99512904 | ||||||
chr4:99513288
|
C | T | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.127+80C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513288 | ||||||
chr4:99513402
|
C | T | 25 | a0001c0001t0001g0250a0002c0004t0001g0028a0002c0004t0001g0247others(22): Show | 26 | HG01074.hp1 HG01346.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.127+194C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513402 | ||||||
chr4:99513453
|
G | C | 1 | a0002c0004t0001g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.127+245G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513453 | ||||||
chr4:99513512
|
G | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 293 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.127+304G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513512 | ||||||
chr4:99513629
|
C | G | 16 | a0003c0002t0001g0282a0005c0006t0001g0029a0005c0006t0001g0030others(13): Show | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.127+421C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513629 | ||||||
chr4:99513642
|
C | T | 43 | a0001c0001t0001g0285a0002c0003t0001g0007a0002c0003t0001g0031others(40): Show | 46 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.127+434C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513642 | ||||||
chr4:99513668
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.127+460C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513668 | ||||||
chr4:99513795
|
C | T | 31 | a0001c0001t0001g0021a0001c0001t0001g0140a0001c0001t0001g0141others(28): Show | 32 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.127+587C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513795 | ||||||
chr4:99513915
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(28): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.127+707C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513915 | ||||||
chr4:99513929
|
A | T | 3 | a0001c0001t0001g0326a0002c0003t0001g0324a0002c0004t0001g0325 | 3 | HG02145.hp1 HG02257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.127+721A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513929 | ||||||
chr4:99513931
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127+723A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99513931 | ||||||
chr4:99514202
|
A | G | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+994A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514202 | ||||||
chr4:99514408
|
G | GA | 29 | a0001c0001t0001g0326a0002c0003t0001g0103a0002c0003t0001g0324others(26): Show | 31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1207dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99514408 | |||||
chr4:99514435
|
G | T | 43 | a0001c0001t0001g0285a0002c0003t0001g0007a0002c0003t0001g0031others(40): Show | 46 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.127+1227G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514435 | ||||||
chr4:99514474
|
T | G | 2 | a0002c0004t0001g0248a0002c0004t0001g0249 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.127+1266T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514474 | ||||||
chr4:99514583
|
T | A | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+1375T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514583 | ||||||
chr4:99514642
|
A | G | 1 | a0002c0003t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127+1434A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514642 | ||||||
chr4:99514669
|
G | A | 29 | a0001c0001t0001g0326a0002c0003t0001g0103a0002c0003t0001g0324others(26): Show | 31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1461G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514669 | ||||||
chr4:99514745
|
C | T | 1 | a0002c0007t0001g0323 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127+1537C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514745 | ||||||
chr4:99514894
|
T | C | 29 | a0001c0001t0001g0326a0002c0003t0001g0103a0002c0003t0001g0324others(26): Show | 31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1686T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514894 | ||||||
chr4:99514910
|
C | T | 29 | a0001c0001t0001g0326a0002c0003t0001g0103a0002c0003t0001g0324others(26): Show | 31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1702C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514910 | ||||||
chr4:99514997
|
C | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(28): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.127+1789C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99514997 | ||||||
chr4:99515075
|
T | A | 29 | a0001c0001t0001g0326a0002c0003t0001g0103a0002c0003t0001g0324others(26): Show | 31 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.127+1867T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515075 | ||||||
chr4:99515180
|
T | C | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127+1972T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515180 | ||||||
chr4:99515197
|
A | G | 31 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(28): Show | 61 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.127+1989A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515197 | ||||||
chr4:99515220
|
C | A | 1 | a0004c0005t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127+2012C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515220 | ||||||
chr4:99515262
|
C | G | 78 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(75): Show | 89 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127+2054C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515262 | ||||||
chr4:99515356
|
C | T | 1 | a0002c0004t0001g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127+2148C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515356 | ||||||
chr4:99515560
|
G | A | 2 | a0003c0002t0001g0170a0003c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.127+2352G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515560 | ||||||
chr4:99515788
|
A | T | 1 | a0002c0003t0001g0322 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.127+2580A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515788 | ||||||
chr4:99515887
|
T | C | 27 | a0002c0003t0001g0103a0002c0004t0001g0032a0002c0004t0001g0033others(24): Show | 29 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+2679T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515887 | ||||||
chr4:99515949
|
C | G | 1 | a0002c0003t0001g0321 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.127+2741C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99515949 | ||||||
chr4:99516068
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.127+2860C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516068 | ||||||
chr4:99516279
|
T | C | 23 | a0002c0003t0001g0103a0002c0004t0001g0062a0002c0004t0001g0063others(20): Show | 25 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.127+3071T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516279 | ||||||
chr4:99516310
|
A | G | 1 | a0004c0005t0001g0059 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.127+3102A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516310 | ||||||
chr4:99516396
|
T | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(75): Show | 89 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.127+3188T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516396 | ||||||
chr4:99516404
|
G | A | 2 | a0003c0002t0001g0006a0003c0002t0001g0172 | 4 | NA18946.hp1 NA18956.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+3196G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516404 | ||||||
chr4:99516407
|
A | C | 1 | a0003c0002t0001g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127+3199A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516407 | ||||||
chr4:99516479
|
G | A | 2 | a0001c0001t0001g0108a0002c0004t0001g0104 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.127+3271G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516479 | ||||||
chr4:99516522
|
G | A | 1 | a0004c0005t0001g0036 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.127+3314G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516522 | ||||||
chr4:99516644
|
A | G | 27 | a0002c0003t0001g0103a0002c0004t0001g0032a0002c0004t0001g0033others(24): Show | 29 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+3436A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516644 | ||||||
chr4:99516730
|
G | A | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.127+3522G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516730 | ||||||
chr4:99516943
|
C | T | 1 | a0004c0005t0001g0058 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127+3735C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99516943 | ||||||
chr4:99516983
|
G | GA | 12 | a0004c0005t0001g0008a0004c0005t0001g0037a0004c0005t0001g0038others(9): Show | 13 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.127+3778dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99516983 | |||||
chr4:99517028
|
G | A | 1 | a0002c0004t0001g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.127+3820G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517028 | ||||||
chr4:99517041
|
G | A | 1 | a0004c0005t0001g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.127+3833G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517041 | ||||||
chr4:99517172
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(70): Show | 106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.127+3964C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517172 | ||||||
chr4:99517329
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 275 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.127+4121A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517329 | ||||||
chr4:99517500
|
C | T | 2 | a0002c0003t0001g0095a0002c0003t0001g0324 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.127+4292C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517500 | ||||||
chr4:99517543
|
CTCTCTTT others(7): Show |
C | 27 | a0003c0002t0001g0050a0004c0005t0001g0008a0004c0005t0001g0009others(24): Show | 29 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.127+4344_127+4357d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99517543 | |||||
chr4:99517578
|
T | TA | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.127+4376dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99517578 | |||||
chr4:99517888
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.128-4612G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517888 | ||||||
chr4:99517919
|
C | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.128-4581C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517919 | ||||||
chr4:99517952
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.128-4548A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517952 | ||||||
chr4:99517995
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.128-4505C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99517995 | ||||||
chr4:99518159
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.128-4341C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518159 | ||||||
chr4:99518194
|
C | T | 2 | a0003c0002t0001g0170a0003c0002t0001g0171 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.128-4306C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518194 | ||||||
chr4:99518249
|
T | G | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG00280.hp1 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.128-4251T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518249 | ||||||
chr4:99518301
|
C | T | 1 | a0002c0004t0001g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.128-4199C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518301 | ||||||
chr4:99518485
|
TA | T | 8 | a0002c0003t0001g0316a0002c0004t0001g0254a0003c0002t0001g0050others(5): Show | 9 | HG00438.hp2 HG01167.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-3981delA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAA | T | 8 | a0001c0001t0001g0174a0001c0001t0001g0234a0002c0003t0001g0318others(5): Show | 8 | HG00733.hp2 HG02109.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-3982_128-3981d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAA | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0112others(8): Show | 12 | HG01243.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.128-3983_128-3981d others(5): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAA | T | 23 | a0001c0001t0001g0120a0001c0001t0001g0130a0001c0001t0001g0131others(20): Show | 23 | HG00558.hp2 HG00621.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.128-3985_128-3981d others(7): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAA | T | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0113others(5): Show | 8 | HG00639.hp1 HG01175.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.128-3986_128-3981d others(8): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0068others(28): Show | 40 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.128-3987_128-3981d others(9): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(1): Show |
T | 18 | a0001c0001t0001g0019a0001c0001t0001g0070a0001c0001t0001g0108others(15): Show | 19 | HG00639.hp2 HG01099.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.128-3988_128-3981d others(10): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(2): Show |
T | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(44): Show | 77 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.128-3989_128-3981d others(11): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(3): Show |
T | 22 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0080others(19): Show | 25 | HG00280.hp1 HG00280.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.128-3990_128-3981d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(4): Show |
T | 10 | a0001c0001t0001g0005a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 13 | HG01070.hp1 HG01071.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.128-3991_128-3981d others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(5): Show |
T | 5 | a0001c0001t0001g0087a0002c0004t0001g0063a0002c0004t0001g0325others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-3992_128-3981d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(6): Show |
T | 1 | a0005c0006t0001g0271 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.128-3993_128-3981d others(15): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(7): Show |
T | 6 | a0005c0006t0001g0030a0005c0006t0001g0273a0005c0006t0001g0274others(3): Show | 7 | HG01884.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3994_128-3981d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(8): Show |
T | 1 | a0005c0006t0001g0279 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.128-3995_128-3981d others(17): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518485
|
TAAAAAAA others(9): Show |
T | 3 | a0002c0003t0001g0103a0005c0006t0001g0280a0005c0006t0001g0281 | 3 | HG03225.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.128-3996_128-3981d others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518485 | |||||
chr4:99518503
|
AAAAAAAA others(10): Show |
A | 1 | a0005c0006t0001g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128-3995_128-3979d others(19): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518503 | |||||
chr4:99518504
|
AAAAAAAA others(9): Show |
A | 1 | a0005c0006t0001g0272 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.128-3994_128-3979d others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518504 | |||||
chr4:99518505
|
AAAAAAAA others(8): Show |
A | 3 | a0002c0003t0001g0324a0002c0009t0001g0102a0005c0006t0001g0029 | 4 | HG02258.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3993_128-3979d others(17): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518505 | |||||
chr4:99518505
|
AAAAAAAA others(10): Show |
A | 1 | a0002c0009t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.128-3993_128-3977d others(19): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518505 | |||||
chr4:99518506
|
A | ATATATAT others(4): Show |
1 | a0002c0004t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.128-3994_128-3993i others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518506 | ||||||
chr4:99518506
|
A | T | 1 | a0002c0003t0001g0319 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128-3994A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518506 | ||||||
chr4:99518507
|
AAAAAAAA others(6): Show |
A | 1 | a0002c0004t0001g0243 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.128-3991_128-3979d others(15): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518507 | |||||
chr4:99518507
|
AAAAAAAA others(8): Show |
A | 2 | a0002c0003t0001g0095a0002c0004t0001g0173 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.128-3991_128-3977d others(17): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518507 | |||||
chr4:99518507
|
AAAAAAAA others(12): Show |
A | 1 | a0002c0009t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128-3991_128-3973d others(21): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518507 | |||||
chr4:99518508
|
A | AT | 3 | a0002c0004t0001g0247a0002c0004t0001g0265a0002c0004t0001g0266 | 3 | HG01074.hp1 HG03453.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.128-3992_128-3991i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518508 | ||||||
chr4:99518508
|
A | T | 7 | a0002c0003t0001g0305a0002c0003t0001g0306a0002c0003t0001g0316others(4): Show | 7 | HG02809.hp1 HG02818.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3992A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518508 | ||||||
chr4:99518508
|
AAAAAAAA others(5): Show |
A | 2 | a0002c0004t0001g0263a0005c0006t0001g0061 | 2 | HG02897.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.128-3990_128-3979d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518508 | |||||
chr4:99518508
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0079 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.128-3990_128-3977d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518508 | |||||
chr4:99518509
|
AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0001g0071a0001c0001t0001g0148a0002c0004t0001g0028others(2): Show | 6 | HG02071.hp1 HG02735.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3989_128-3979d others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518509 | |||||
chr4:99518510
|
A | T | 19 | a0002c0003t0001g0065a0002c0003t0001g0293a0002c0003t0001g0294others(16): Show | 19 | HG01074.hp1 HG01243.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.128-3990A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518510 | ||||||
chr4:99518510
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0116 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.128-3988_128-3979d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518510 | |||||
chr4:99518511
|
AAAAAAAA others(2): Show |
A | 6 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0143others(3): Show | 7 | HG01975.hp1 HG02451.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-3987_128-3979d others(11): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518511 | |||||
chr4:99518512
|
A | T | 35 | a0002c0003t0001g0065a0002c0003t0001g0293a0002c0003t0001g0294others(32): Show | 35 | HG00639.hp2 HG01070.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.128-3988A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518512 | ||||||
chr4:99518512
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.128-3986_128-3977d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518512 | |||||
chr4:99518514
|
A | AT | 9 | a0003c0002t0001g0211a0003c0002t0001g0212a0003c0002t0001g0214others(6): Show | 9 | HG02015.hp1 HG02056.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.128-3986_128-3985i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518514 | ||||||
chr4:99518514
|
A | ATATATAT others(4): Show |
1 | a0003c0008t0001g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.128-3986_128-3985i others(13): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518514 | ||||||
chr4:99518514
|
A | T | 51 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0234others(48): Show | 51 | HG00621.hp1 HG00639.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.128-3986A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518514 | ||||||
chr4:99518516
|
A | AT | 7 | a0003c0002t0001g0170a0003c0002t0001g0198a0003c0002t0001g0199others(4): Show | 7 | HG00733.hp1 HG02602.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3984_128-3983i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518516 | ||||||
chr4:99518516
|
A | ATAT | 4 | a0003c0002t0001g0197a0003c0002t0001g0201a0003c0002t0001g0202others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3984_128-3983i others(5): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518516 | ||||||
chr4:99518516
|
A | T | 93 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0130others(90): Show | 94 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.128-3984A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518516 | ||||||
chr4:99518518
|
A | AATATATA others(3): Show |
1 | a0003c0002t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.128-3964_128-3955d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518518 | |||||
chr4:99518518
|
A | AT | 3 | a0003c0002t0001g0022a0003c0002t0001g0186a0003c0002t0001g0327 | 4 | HG02040.hp1 HG02735.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3982_128-3981i others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518518 | ||||||
chr4:99518518
|
A | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(167): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.128-3982A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518518 | ||||||
chr4:99518538
|
T | G | 2 | a0003c0002t0001g0211a0004c0005t0001g0057 | 2 | HG02717.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.128-3962T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518538 | ||||||
chr4:99518540
|
T | G | 9 | a0001c0001t0001g0139a0002c0004t0001g0262a0003c0002t0001g0187others(6): Show | 9 | HG01192.hp1 HG02056.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-3960T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518540 | ||||||
chr4:99518542
|
T | G | 22 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0139others(19): Show | 22 | HG00140.hp1 HG00544.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.128-3958T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518542 | ||||||
chr4:99518542
|
T | TAGAGAGA others(7): Show |
1 | a0002c0004t0001g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-3957_128-3956i others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518542 | |||||
chr4:99518544
|
T | G | 50 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0110others(47): Show | 50 | HG00140.hp1 HG00544.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-3956T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518544 | ||||||
chr4:99518544
|
T | TAGAG | 4 | a0002c0004t0001g0267a0003c0002t0001g0201a0004c0005t0001g0055others(1): Show | 4 | HG02132.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3919_128-3916d others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
T | TAGAGAGA others(3): Show |
1 | a0003c0008t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.128-3925_128-3916d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
T | TATATAGA others(3): Show |
2 | a0003c0002t0001g0193a0003c0002t0001g0226 | 2 | HG02055.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.128-3955_128-3954i others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
T | TATATATA others(9): Show |
1 | a0003c0008t0001g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128-3955_128-3954i others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
T | TATATATA others(5): Show |
1 | a0003c0002t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.128-3955_128-3954i others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
TAGAG | T | 9 | a0001c0001t0001g0142a0002c0004t0001g0027a0002c0004t0001g0104others(6): Show | 10 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-3919_128-3916d others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
TAGAGAG | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0087a0002c0004t0001g0253others(8): Show | 12 | HG01168.hp2 HG01975.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.128-3921_128-3916d others(8): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
TAGAGAGA others(1): Show |
T | 16 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0071others(13): Show | 20 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-3923_128-3916d others(10): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
TAGAGAGA others(3): Show |
T | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(20): Show | 50 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.128-3925_128-3916d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518544
|
TAGAGAGA others(5): Show |
T | 5 | a0001c0001t0001g0017a0001c0001t0001g0069a0001c0001t0001g0326others(2): Show | 6 | HG00408.hp1 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3927_128-3916d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518544 | |||||
chr4:99518546
|
G | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(137): Show | 157 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.128-3954G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518546 | ||||||
chr4:99518548
|
G | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(92): Show | 110 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.128-3952G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518548 | ||||||
chr4:99518550
|
G | T | 55 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0108others(52): Show | 62 | HG00140.hp2 HG00558.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-3950G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518550 | ||||||
chr4:99518552
|
G | T | 21 | a0001c0001t0001g0020a0001c0001t0001g0087a0001c0001t0001g0114others(18): Show | 23 | HG00140.hp2 HG01070.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.128-3948G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518552 | ||||||
chr4:99518554
|
G | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0082others(18): Show | 25 | HG01081.hp2 HG02486.hp1 HG02523.hp1 others(22): Show |
intron_variant | MODIFIER | c.128-3946G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518554 | ||||||
chr4:99518556
|
G | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(22): Show | 47 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.128-3944G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518556 | ||||||
chr4:99518558
|
G | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0069others(5): Show | 10 | HG00408.hp1 HG00544.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.128-3942G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518558 | ||||||
chr4:99518560
|
G | T | 1 | a0001c0001t0001g0078 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.128-3940G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518560 | ||||||
chr4:99518566
|
G | C | 1 | a0002c0009t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128-3934G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518566 | ||||||
chr4:99518573
|
AGAGAGAG others(9): Show |
A | 2 | a0002c0003t0001g0294a0002c0003t0001g0305 | 2 | HG02809.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.128-3922_128-3907d others(18): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518573 | |||||
chr4:99518574
|
G | C | 1 | a0002c0009t0001g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.128-3926G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518574 | ||||||
chr4:99518575
|
AGAGAGAG others(7): Show |
A | 1 | a0002c0003t0001g0295 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.128-3920_128-3907d others(16): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518575 | |||||
chr4:99518576
|
G | C | 1 | a0002c0009t0001g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.128-3924G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518576 | ||||||
chr4:99518577
|
AGAGAGAG others(5): Show |
A | 1 | a0002c0003t0001g0322 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.128-3918_128-3907d others(14): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518577 | |||||
chr4:99518578
|
G | C | 1 | a0002c0009t0001g0286 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.128-3922G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518578 | ||||||
chr4:99518579
|
AGAGAGGG others(3): Show |
A | 1 | a0002c0003t0001g0306 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.128-3916_128-3907d others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518579 | |||||
chr4:99518581
|
AGAGGGAG others(1): Show |
A | 4 | a0002c0003t0001g0095a0002c0003t0001g0103a0002c0003t0001g0324others(1): Show | 4 | HG02723.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3915_128-3908d others(10): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518581 | |||||
chr4:99518582
|
G | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0094a0002c0004t0001g0062others(17): Show | 23 | HG00735.hp1 HG01884.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.128-3918G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518582 | ||||||
chr4:99518583
|
AGGGAGG | A | 31 | a0002c0003t0001g0007a0002c0003t0001g0031a0002c0003t0001g0064others(28): Show | 34 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.128-3915_128-3910d others(8): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518583 | |||||
chr4:99518585
|
G | A | 6 | a0002c0003t0001g0065a0002c0003t0001g0293a0002c0003t0001g0318others(3): Show | 6 | HG02145.hp2 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.128-3915G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518585 | ||||||
chr4:99518589
|
G | A | 7 | a0002c0003t0001g0065a0002c0003t0001g0293a0002c0003t0001g0318others(4): Show | 7 | HG02145.hp2 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-3911G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518589 | ||||||
chr4:99518730
|
C | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.128-3770C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518730 | ||||||
chr4:99518753
|
A | T | 1 | a0003c0002t0001g0186 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.128-3747A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518753 | ||||||
chr4:99518757
|
G | A | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-3743G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518757 | ||||||
chr4:99518757
|
G | GTC | 28 | a0002c0004t0001g0027a0002c0004t0001g0028a0002c0004t0001g0104others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-3741_128-3740d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99518757 | |||||
chr4:99518879
|
T | C | 4 | a0003c0002t0001g0105a0003c0002t0001g0106a0003c0002t0001g0107others(1): Show | 4 | HG02559.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-3621T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518879 | ||||||
chr4:99518922
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.128-3578T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518922 | ||||||
chr4:99518955
|
G | A | 3 | a0002c0009t0001g0101a0002c0009t0001g0102a0002c0009t0001g0286 | 3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-3545G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99518955 | ||||||
chr4:99519489
|
T | C | 47 | a0002c0003t0001g0007a0002c0003t0001g0031a0002c0003t0001g0064others(44): Show | 50 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.128-3011T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519489 | ||||||
chr4:99519602
|
T | G | 2 | a0002c0004t0001g0173a0002c0004t0001g0243 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.128-2898T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519602 | ||||||
chr4:99519622
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.128-2878G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519622 | ||||||
chr4:99519687
|
G | T | 5 | a0004c0005t0001g0009a0004c0005t0001g0051a0004c0005t0001g0052others(2): Show | 6 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-2813G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519687 | ||||||
chr4:99519688
|
A | T | 1 | a0002c0003t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.128-2812A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519688 | ||||||
chr4:99519762
|
T | A | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG01261.hp2 HG01358.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.128-2738T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519762 | ||||||
chr4:99519794
|
G | C | 1 | a0002c0004t0001g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.128-2706G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519794 | ||||||
chr4:99519826
|
G | A | 1 | a0002c0003t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.128-2674G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99519826 | ||||||
chr4:99520089
|
A | AT | 96 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(93): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.128-2393dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99520089 | |||||
chr4:99520089
|
A | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(29): Show | 62 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-2411A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520089 | ||||||
chr4:99520089
|
AT | A | 47 | a0001c0001t0001g0014a0001c0001t0001g0094a0002c0003t0001g0007others(44): Show | 51 | HG00558.hp2 HG00621.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.128-2393delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99520089 | |||||
chr4:99520092
|
T | A | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(29): Show | 62 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-2408T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520092 | ||||||
chr4:99520096
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.128-2404T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520096 | ||||||
chr4:99520101
|
T | C | 26 | a0004c0005t0001g0008a0004c0005t0001g0009a0004c0005t0001g0036others(23): Show | 28 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.128-2399T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520101 | ||||||
chr4:99520175
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(29): Show | 62 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.128-2325C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520175 | ||||||
chr4:99520235
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.128-2265G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520235 | ||||||
chr4:99520256
|
A | AT | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(192): Show | 245 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.128-2234dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99520256 | |||||
chr4:99520297
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.128-2203G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520297 | ||||||
chr4:99520308
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0108a0001c0001t0001g0110others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.128-2192G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520308 | ||||||
chr4:99520337
|
C | T | 1 | a0002c0004t0001g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128-2163C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520337 | ||||||
chr4:99520371
|
A | C | 1 | a0005c0006t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.128-2129A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520371 | ||||||
chr4:99520649
|
A | G | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-1851A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520649 | ||||||
chr4:99520729
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.128-1771A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520729 | ||||||
chr4:99520840
|
T | C | 2 | a0003c0002t0001g0176a0003c0002t0001g0200 | 2 | HG02698.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.128-1660T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520840 | ||||||
chr4:99520924
|
T | C | 7 | a0002c0004t0001g0255a0002c0004t0001g0256a0002c0004t0001g0258others(4): Show | 7 | HG02735.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-1576T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520924 | ||||||
chr4:99520947
|
T | A | 1 | a0004c0005t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.128-1553T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99520947 | ||||||
chr4:99521004
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0089 | 3 | NA18961.hp2 NA19075.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.128-1496G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521004 | ||||||
chr4:99521101
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18969.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.128-1399C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521101 | ||||||
chr4:99521200
|
C | T | 1 | a0003c0002t0001g0023 | 2 | NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.128-1300C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521200 | ||||||
chr4:99521215
|
T | C | 3 | a0002c0009t0001g0101a0002c0009t0001g0102a0002c0009t0001g0286 | 3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-1285T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521215 | ||||||
chr4:99521332
|
A | G | 1 | a0004c0005t0001g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.128-1168A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521332 | ||||||
chr4:99521374
|
C | CA | 29 | a0001c0001t0001g0250a0002c0003t0001g0318a0002c0004t0001g0265others(26): Show | 31 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.128-1115dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99521374 | |||||
chr4:99521386
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 313 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.128-1114G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521386 | ||||||
chr4:99521421
|
T | C | 1 | a0002c0003t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.128-1079T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521421 | ||||||
chr4:99521539
|
T | G | 3 | a0002c0009t0001g0101a0002c0009t0001g0102a0002c0009t0001g0286 | 3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-961T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521539 | ||||||
chr4:99521559
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(253): Show | 310 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.128-941A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521559 | ||||||
chr4:99521683
|
C | T | 28 | a0002c0004t0001g0027a0002c0004t0001g0028a0002c0004t0001g0104others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-817C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521683 | ||||||
chr4:99521728
|
A | G | 28 | a0001c0001t0001g0155a0001c0001t0001g0163a0004c0005t0001g0008others(25): Show | 30 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.128-772A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521728 | ||||||
chr4:99521774
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.128-726C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521774 | ||||||
chr4:99521784
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.128-716C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521784 | ||||||
chr4:99521804
|
A | G | 7 | a0003c0002t0001g0189a0003c0002t0001g0208a0003c0002t0001g0221others(4): Show | 7 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.128-696A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521804 | ||||||
chr4:99521853
|
G | T | 65 | a0002c0003t0001g0007a0002c0003t0001g0031a0002c0003t0001g0064others(62): Show | 70 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-647G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521853 | ||||||
chr4:99521910
|
G | C | 1 | a0004c0005t0001g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.128-590G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521910 | ||||||
chr4:99521914
|
G | A | 4 | a0002c0004t0001g0032a0002c0004t0001g0033a0002c0004t0001g0034others(1): Show | 4 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.128-586G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521914 | ||||||
chr4:99521986
|
A | G | 62 | a0002c0003t0001g0007a0002c0003t0001g0031a0002c0003t0001g0064others(59): Show | 67 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(64): Show |
intron_variant | MODIFIER | c.128-514A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99521986 | ||||||
chr4:99522197
|
T | TAGAAGGT others(23): Show |
1 | a0001c0001t0001g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.128-301_128-272dup others(30): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522197 | |||||
chr4:99522250
|
C | T | 65 | a0002c0003t0001g0007a0002c0003t0001g0031a0002c0003t0001g0064others(62): Show | 70 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.128-250C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522250 | ||||||
chr4:99522301
|
A | G | 3 | a0002c0009t0001g0101a0002c0009t0001g0102a0002c0009t0001g0286 | 3 | HG02647.hp1 HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.128-199A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522301 | ||||||
chr4:99522347
|
A | AT | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 201 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(198): Show |
intron_variant | MODIFIER | c.128-142dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522347 | |||||
chr4:99522347
|
A | ATT | 10 | a0002c0003t0001g0095a0002c0003t0001g0103a0002c0003t0001g0324others(7): Show | 10 | HG00639.hp2 HG01243.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.128-143_128-142dup others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522347 | |||||
chr4:99522347
|
A | ATTT | 18 | a0002c0004t0001g0062a0002c0004t0001g0063a0005c0006t0001g0029others(15): Show | 20 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-144_128-142dup others(3): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522347 | |||||
chr4:99522357
|
TTGGTTTA others(5): Show |
T | 41 | a0002c0003t0001g0007a0002c0003t0001g0031a0002c0003t0001g0064others(38): Show | 44 | HG00558.hp2 HG00621.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.128-141_128-130del others(12): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99522357 | |||||
chr4:99522370
|
T | C | 18 | a0002c0004t0001g0062a0002c0004t0001g0063a0005c0006t0001g0029others(15): Show | 20 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.128-130T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522370 | ||||||
chr4:99522404
|
A | G | 100 | a0001c0001t0001g0155a0001c0001t0001g0163a0003c0002t0001g0006others(97): Show | 106 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.128-96A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 2/8 | chr4 | 99522404 | ||||||
chr4:99522778
|
A | G | 2 | a0002c0003t0001g0095a0002c0003t0001g0324 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.337+69A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99522778 | ||||||
chr4:99522869
|
A | G | 28 | a0002c0004t0001g0027a0002c0004t0001g0028a0002c0004t0001g0104others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.337+160A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99522869 | ||||||
chr4:99523021
|
T | C | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(146): Show | 188 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.337+312T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523021 | ||||||
chr4:99523062
|
T | TGAAATTG others(937): Show |
1 | a0002c0004t0001g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.337+364_337+365ins others(944): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523062 | |||||
chr4:99523206
|
A | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(70): Show | 106 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.337+497A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523206 | ||||||
chr4:99523250
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.337+541G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523250 | ||||||
chr4:99523278
|
T | TAG | 52 | a0001c0001t0001g0014a0001c0001t0001g0094a0002c0003t0001g0103others(49): Show | 57 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.337+570_337+571ins others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523278 | |||||
chr4:99523527
|
T | C | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(246): Show | 300 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(297): Show |
intron_variant | MODIFIER | c.337+818T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523527 | ||||||
chr4:99523528
|
G | A | 3 | a0002c0004t0001g0028a0002c0004t0001g0253a0002c0004t0001g0263 | 4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+819G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523528 | ||||||
chr4:99523610
|
A | G | 102 | a0001c0001t0001g0326a0002c0003t0001g0298a0002c0003t0001g0324others(99): Show | 108 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.337+901A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523610 | ||||||
chr4:99523681
|
T | C | 11 | a0001c0001t0001g0014a0001c0001t0001g0094a0001c0001t0001g0326others(8): Show | 12 | HG00639.hp2 HG00735.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.338-840T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523681 | ||||||
chr4:99523755
|
T | C | 1 | a0002c0004t0001g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.338-766T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523755 | ||||||
chr4:99523775
|
C | T | 1 | a0002c0003t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338-746C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523775 | ||||||
chr4:99523885
|
T | C | 1 | a0002c0003t0001g0319 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.338-636T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523885 | ||||||
chr4:99523906
|
T | C | 19 | a0002c0003t0001g0095a0002c0004t0001g0033a0002c0004t0001g0034others(16): Show | 21 | HG00639.hp2 HG01257.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.338-615T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523906 | ||||||
chr4:99523907
|
T | C | 2 | a0005c0006t0001g0029a0005c0006t0001g0271 | 3 | HG02258.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.338-614T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523907 | ||||||
chr4:99523974
|
T | C | 1 | a0004c0005t0001g0041 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.338-547T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523974 | ||||||
chr4:99523975
|
A | C | 1 | a0002c0003t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338-546A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99523975 | ||||||
chr4:99523976
|
C | CT | 16 | a0001c0001t0001g0127a0001c0001t0001g0144a0001c0001t0001g0145others(13): Show | 16 | HG01071.hp1 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.338-524dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523976 | |||||
chr4:99523976
|
CT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 141 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.338-524delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523976 | |||||
chr4:99523976
|
CTT | C | 44 | a0001c0001t0001g0169a0002c0004t0001g0032a0003c0008t0001g0091others(41): Show | 48 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.338-525_338-524del others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99523976 | |||||
chr4:99524010
|
T | C | 16 | a0005c0006t0001g0029a0005c0006t0001g0030a0005c0006t0001g0061others(13): Show | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.338-511T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524010 | ||||||
chr4:99524081
|
G | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0083others(83): Show | 97 | HG00558.hp2 HG00621.hp1 HG01070.hp1 others(94): Show |
intron_variant | MODIFIER | c.338-440G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524081 | ||||||
chr4:99524092
|
G | A | 1 | a0002c0003t0001g0306 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.338-429G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524092 | ||||||
chr4:99524125
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 213 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.338-396G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524125 | ||||||
chr4:99524136
|
C | T | 1 | a0002c0004t0001g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.338-385C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524136 | ||||||
chr4:99524140
|
C | T | 16 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(13): Show | 16 | HG00741.hp1 HG01106.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.338-381C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524140 | ||||||
chr4:99524192
|
A | G | 1 | a0004c0005t0001g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.338-329A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524192 | ||||||
chr4:99524202
|
C | T | 32 | a0001c0001t0001g0110a0002c0003t0001g0095a0002c0003t0001g0315others(29): Show | 33 | HG00438.hp2 HG00558.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.338-319C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524202 | ||||||
chr4:99524227
|
C | T | 1 | a0002c0003t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338-294C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524227 | ||||||
chr4:99524241
|
T | A | 1 | a0001c0001t0001g0014 | 2 | HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.338-280T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524241 | ||||||
chr4:99524291
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.338-230C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524291 | ||||||
chr4:99524432
|
T | TC | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 289 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(286): Show |
intron_variant | MODIFIER | c.338-89_338-88insC | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524432 | ||||||
chr4:99524472
|
A | G | 1 | a0003c0002t0001g0327 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.338-49A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 3/8 | chr4 | 99524472 | ||||||
chr4:99524606
|
GCTAT | G | 78 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(75): Show | 85 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.402+26_402+29delCT others(2): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99524606 | |||||
chr4:99524629
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(58): Show | 70 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.402+44A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524629 | ||||||
chr4:99524704
|
A | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0156others(3): Show | 6 | HG01071.hp1 HG02300.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+119A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524704 | ||||||
chr4:99524733
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+148A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524733 | ||||||
chr4:99524809
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0108a0001c0001t0001g0111others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+224C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99524809 | ||||||
chr4:99525022
|
C | A | 2 | a0002c0003t0001g0095a0002c0003t0001g0324 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.402+437C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525022 | ||||||
chr4:99525154
|
G | C | 1 | a0003c0002t0001g0185 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.402+569G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525154 | ||||||
chr4:99525282
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.402+697C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525282 | ||||||
chr4:99525286
|
C | T | 1 | a0004c0005t0001g0047 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.402+701C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525286 | ||||||
chr4:99525302
|
T | A | 21 | a0001c0001t0001g0014a0002c0003t0001g0308a0002c0003t0001g0318others(18): Show | 22 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.402+717T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525302 | ||||||
chr4:99525322
|
C | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(59): Show | 71 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.402+737C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525322 | ||||||
chr4:99525795
|
CA | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0113others(3): Show | 7 | HG00639.hp1 HG02896.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+1224delA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99525795 | |||||
chr4:99525976
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+1391C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99525976 | ||||||
chr4:99526076
|
C | T | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.402+1491C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526076 | ||||||
chr4:99526096
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.402+1511G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526096 | ||||||
chr4:99526111
|
A | G | 2 | a0003c0002t0001g0224a0003c0002t0001g0225 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.402+1526A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526111 | ||||||
chr4:99526164
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+1579C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526164 | ||||||
chr4:99526298
|
T | C | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.402+1713T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526298 | ||||||
chr4:99526362
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.402+1777A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526362 | ||||||
chr4:99526458
|
G | A | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.402+1873G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526458 | ||||||
chr4:99526643
|
T | C | 3 | a0002c0004t0001g0027a0002c0004t0001g0173a0002c0004t0001g0243 | 4 | HG01070.hp1 HG01071.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+2058T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526643 | ||||||
chr4:99526651
|
C | CT | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 163 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.402+2080dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99526651 | |||||
chr4:99526651
|
C | CTT | 19 | a0002c0004t0001g0262a0003c0002t0001g0184a0004c0005t0001g0042others(16): Show | 21 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+2079_402+2080d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99526651 | |||||
chr4:99526740
|
T | C | 3 | a0001c0001t0001g0094a0001c0001t0001g0326a0002c0003t0001g0103 | 3 | HG00735.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.402+2155T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526740 | ||||||
chr4:99526848
|
C | T | 1 | a0004c0005t0001g0057 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.402+2263C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526848 | ||||||
chr4:99526913
|
T | C | 3 | a0002c0004t0001g0028a0002c0004t0001g0253a0002c0004t0001g0263 | 4 | HG02896.hp2 HG02897.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+2328T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526913 | ||||||
chr4:99526964
|
T | G | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.402+2379T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99526964 | ||||||
chr4:99527010
|
G | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 290 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(287): Show |
intron_variant | MODIFIER | c.402+2425G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527010 | ||||||
chr4:99527065
|
C | G | 82 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(79): Show | 89 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.402+2480C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527065 | ||||||
chr4:99527104
|
C | T | 11 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 14 | HG01074.hp2 HG01255.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.402+2519C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527104 | ||||||
chr4:99527383
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0155a0001c0001t0001g0163 | 3 | HG01099.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.403-2432A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527383 | ||||||
chr4:99527501
|
G | C | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.403-2314G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527501 | ||||||
chr4:99527575
|
C | T | 1 | a0002c0004t0001g0033 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.403-2240C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527575 | ||||||
chr4:99527584
|
C | T | 1 | a0002c0004t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.403-2231C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527584 | ||||||
chr4:99527588
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-2227C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527588 | ||||||
chr4:99527667
|
C | T | 87 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(84): Show | 96 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.403-2148C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527667 | ||||||
chr4:99527702
|
C | T | 1 | a0002c0003t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.403-2113C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527702 | ||||||
chr4:99527713
|
C | G | 1 | a0002c0003t0001g0312 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.403-2102C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527713 | ||||||
chr4:99527820
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.403-1995G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527820 | ||||||
chr4:99527933
|
C | G | 1 | a0003c0002t0001g0219 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.403-1882C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99527933 | ||||||
chr4:99528195
|
T | C | 1 | a0004c0005t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.403-1620T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528195 | ||||||
chr4:99528208
|
TAAAAG | T | 70 | a0001c0001t0001g0068a0001c0001t0001g0110a0002c0003t0001g0095others(67): Show | 76 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.403-1604_403-1600d others(7): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99528208 | |||||
chr4:99528212
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.403-1603A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528212 | ||||||
chr4:99528256
|
G | C | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.403-1559G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528256 | ||||||
chr4:99528352
|
CTCTT | C | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.403-1459_403-1456d others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99528352 | |||||
chr4:99528532
|
T | G | 16 | a0005c0006t0001g0029a0005c0006t0001g0030a0005c0006t0001g0061others(13): Show | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.403-1283T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528532 | ||||||
chr4:99528543
|
C | G | 16 | a0005c0006t0001g0029a0005c0006t0001g0030a0005c0006t0001g0061others(13): Show | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.403-1272C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528543 | ||||||
chr4:99528578
|
A | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.403-1237A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528578 | ||||||
chr4:99528709
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.403-1106G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528709 | ||||||
chr4:99528794
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0133 | 2 | HG01346.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.403-1021C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528794 | ||||||
chr4:99528794
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.403-1021C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528794 | ||||||
chr4:99528816
|
C | A | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.403-999C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528816 | ||||||
chr4:99528840
|
T | C | 82 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(79): Show | 89 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.403-975T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99528840 | ||||||
chr4:99528922
|
AT | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0326a0002c0003t0001g0103 | 3 | HG00735.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.403-890delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99528922 | |||||
chr4:99529099
|
A | G | 1 | a0004c0005t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403-716A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529099 | ||||||
chr4:99529536
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.403-279A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529536 | ||||||
chr4:99529555
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 182 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.403-260C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529555 | ||||||
chr4:99529616
|
A | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.403-199A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529616 | ||||||
chr4:99529800
|
A | G | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.403-15A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 4/8 | chr4 | 99529800 | ||||||
chr4:99529970
|
G | A | 64 | a0001c0001t0001g0068a0001c0001t0001g0110a0002c0003t0001g0298others(61): Show | 70 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.546+12G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99529970 | ||||||
chr4:99530036
|
A | T | 1 | a0003c0002t0001g0208 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.546+78A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530036 | ||||||
chr4:99530040
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+82C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530040 | ||||||
chr4:99530210
|
C | A | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.546+252C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530210 | ||||||
chr4:99530218
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(237): Show | 291 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+260A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530218 | ||||||
chr4:99530230
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+272C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530230 | ||||||
chr4:99530238
|
C | T | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.546+280C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530238 | ||||||
chr4:99530265
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0108a0001c0001t0001g0111others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+307A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530265 | ||||||
chr4:99530299
|
T | C | 1 | a0004c0005t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.546+341T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530299 | ||||||
chr4:99530360
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+402C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530360 | ||||||
chr4:99530452
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.546+494G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530452 | ||||||
chr4:99530527
|
A | AT | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+575dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99530527 | |||||
chr4:99530624
|
C | T | 2 | a0002c0004t0001g0034a0002c0004t0001g0035 | 2 | HG00639.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.546+666C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530624 | ||||||
chr4:99530663
|
A | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+705A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530663 | ||||||
chr4:99530784
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 109 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.546+826A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530784 | ||||||
chr4:99530792
|
AGAATAAA others(2): Show |
A | 3 | a0004c0005t0001g0008a0004c0005t0001g0037a0004c0005t0001g0040 | 4 | HG01891.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+838_546+846del others(9): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99530792 | |||||
chr4:99530978
|
C | T | 1 | a0005c0006t0001g0272 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.546+1020C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99530978 | ||||||
chr4:99531005
|
G | T | 16 | a0005c0006t0001g0029a0005c0006t0001g0030a0005c0006t0001g0061others(13): Show | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.546+1047G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531005 | ||||||
chr4:99531122
|
G | GT | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+1173dupT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531122 | |||||
chr4:99531122
|
GT | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(103): Show | 141 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.546+1173delT | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531122 | |||||
chr4:99531191
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.546+1233T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531191 | ||||||
chr4:99531224
|
A | G | 1 | a0002c0003t0001g0319 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.546+1266A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531224 | ||||||
chr4:99531290
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.546+1332C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531290 | ||||||
chr4:99531506
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.546+1548G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531506 | ||||||
chr4:99531555
|
A | G | 8 | a0002c0004t0001g0032a0003c0002t0001g0189a0003c0002t0001g0208others(5): Show | 8 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.546+1597A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531555 | ||||||
chr4:99531630
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.546+1672C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531630 | ||||||
chr4:99531729
|
C | G | 2 | a0001c0001t0001g0094a0002c0003t0001g0103 | 2 | HG00735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.546+1771C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531729 | ||||||
chr4:99531804
|
C | T | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.546+1846C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531804 | ||||||
chr4:99531854
|
C | CA | 181 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 200 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(197): Show |
intron_variant | MODIFIER | c.546+1903dupA | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531854 | |||||
chr4:99531854
|
C | CAA | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(56): Show | 91 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.546+1902_546+1903d others(4): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99531854 | |||||
chr4:99531887
|
T | C | 2 | a0002c0004t0001g0173a0002c0004t0001g0243 | 2 | HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.546+1929T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99531887 | ||||||
chr4:99532067
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.546+2109A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532067 | ||||||
chr4:99532080
|
T | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.546+2122T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532080 | ||||||
chr4:99532304
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.546+2346T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532304 | ||||||
chr4:99532348
|
C | T | 2 | a0002c0004t0001g0258a0003c0002t0001g0175 | 2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.546+2390C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532348 | ||||||
chr4:99532419
|
G | T | 58 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(55): Show | 67 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.546+2461G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532419 | ||||||
chr4:99532589
|
C | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 294 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(291): Show |
intron_variant | MODIFIER | c.546+2631C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532589 | ||||||
chr4:99532611
|
G | A | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.546+2653G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532611 | ||||||
chr4:99532768
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.546+2810G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99532768 | ||||||
chr4:99533496
|
A | C | 1 | a0002c0004t0001g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.546+3538A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99533496 | ||||||
chr4:99533582
|
G | T | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.546+3624G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99533582 | ||||||
chr4:99533808
|
CG | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.546+3853delG | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99533808 | |||||
chr4:99534002
|
G | A | 70 | a0001c0001t0001g0068a0001c0001t0001g0110a0002c0003t0001g0095others(67): Show | 76 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.547-3667G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534002 | ||||||
chr4:99534010
|
T | C | 1 | a0002c0003t0001g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547-3659T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534010 | ||||||
chr4:99534012
|
T | G | 4 | a0002c0007t0001g0296a0002c0007t0001g0307a0002c0007t0001g0320others(1): Show | 4 | HG02145.hp2 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-3657T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534012 | ||||||
chr4:99534044
|
T | C | 1 | a0003c0002t0001g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-3625T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534044 | ||||||
chr4:99534347
|
A | G | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.547-3322A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534347 | ||||||
chr4:99534413
|
C | T | 21 | a0001c0001t0001g0014a0002c0003t0001g0308a0002c0003t0001g0318others(18): Show | 22 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.547-3256C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534413 | ||||||
chr4:99534719
|
C | T | 1 | a0002c0003t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.547-2950C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534719 | ||||||
chr4:99534837
|
G | A | 1 | a0003c0002t0001g0219 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.547-2832G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534837 | ||||||
chr4:99534925
|
A | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.547-2744A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99534925 | ||||||
chr4:99535033
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0326a0002c0003t0001g0103 | 3 | HG00735.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.547-2636C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535033 | ||||||
chr4:99535075
|
C | T | 63 | a0001c0001t0001g0110a0002c0003t0001g0298a0002c0004t0001g0027others(60): Show | 69 | HG00544.hp1 HG00741.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.547-2594C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535075 | ||||||
chr4:99535122
|
C | T | 46 | a0002c0003t0001g0298a0002c0004t0001g0247a0002c0004t0001g0248others(43): Show | 50 | HG00544.hp1 HG00741.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.547-2547C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535122 | ||||||
chr4:99535151
|
C | T | 1 | a0004c0005t0001g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.547-2518C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535151 | ||||||
chr4:99535180
|
G | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01516.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.547-2489G>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535180 | ||||||
chr4:99535280
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0108a0001c0001t0001g0111others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.547-2389C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535280 | ||||||
chr4:99535311
|
G | A | 4 | a0003c0002t0001g0105a0003c0002t0001g0106a0003c0002t0001g0107others(1): Show | 4 | HG02559.hp1 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2358G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535311 | ||||||
chr4:99535330
|
T | TTTTCCAA others(21): Show |
1 | a0001c0001t0001g0074 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.547-2337_547-2310d others(30): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99535330 | |||||
chr4:99535408
|
C | G | 3 | a0002c0004t0001g0027a0002c0004t0001g0173a0002c0004t0001g0243 | 4 | HG01070.hp1 HG01071.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2261C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535408 | ||||||
chr4:99535417
|
C | T | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.547-2252C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535417 | ||||||
chr4:99535592
|
A | G | 16 | a0005c0006t0001g0029a0005c0006t0001g0030a0005c0006t0001g0061others(13): Show | 18 | HG01884.hp2 HG01975.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.547-2077A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535592 | ||||||
chr4:99535677
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.547-1992C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535677 | ||||||
chr4:99535744
|
A | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0160a0003c0002t0001g0176others(3): Show | 6 | HG00140.hp2 HG01168.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1925A>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535744 | ||||||
chr4:99535845
|
T | C | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.547-1824T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99535845 | ||||||
chr4:99535960
|
A | ACAGT | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-1706_547-1705i others(6): Show |
C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99535960 | |||||
chr4:99536119
|
G | A | 1 | a0003c0002t0001g0106 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.547-1550G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536119 | ||||||
chr4:99536187
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-1482C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536187 | ||||||
chr4:99536215
|
C | A | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.547-1454C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536215 | ||||||
chr4:99536275
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.547-1394C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536275 | ||||||
chr4:99536471
|
A | G | 1 | a0002c0004t0001g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.547-1198A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536471 | ||||||
chr4:99536529
|
G | T | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.547-1140G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536529 | ||||||
chr4:99536533
|
C | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 182 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.547-1136C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536533 | ||||||
chr4:99536684
|
T | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-985T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536684 | ||||||
chr4:99536690
|
A | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0151 | 2 | HG01081.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.547-979A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536690 | ||||||
chr4:99536783
|
G | A | 1 | a0004c0005t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.547-886G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536783 | ||||||
chr4:99536988
|
C | G | 1 | a0002c0003t0001g0310 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.547-681C>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99536988 | ||||||
chr4:99537008
|
C | T | 1 | a0003c0002t0001g0050 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.547-661C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537008 | ||||||
chr4:99537245
|
TG | T | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.547-423delG | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537245 | ||||||
chr4:99537267
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.547-402G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537267 | ||||||
chr4:99537291
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.547-378A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537291 | ||||||
chr4:99537404
|
G | T | 60 | a0001c0001t0001g0110a0002c0003t0001g0298a0002c0004t0001g0028others(57): Show | 65 | HG00544.hp1 HG00741.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.547-265G>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537404 | ||||||
chr4:99537506
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.547-163G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537506 | ||||||
chr4:99537564
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.547-105T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537564 | ||||||
chr4:99537616
|
A | G | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.547-53A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 5/8 | chr4 | 99537616 | ||||||
chr4:99537836
|
T | C | 3 | a0002c0004t0001g0255a0002c0004t0001g0256a0002c0004t0001g0284 | 3 | HG03491.hp1 HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.628+86T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99537836 | ||||||
chr4:99537871
|
C | T | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.628+121C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99537871 | ||||||
chr4:99538189
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.628+439C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538189 | ||||||
chr4:99538398
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.628+648G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538398 | ||||||
chr4:99538516
|
T | G | 1 | a0004c0005t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.629-647T>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538516 | ||||||
chr4:99538538
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.629-625C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538538 | ||||||
chr4:99538595
|
C | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.629-568C>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538595 | ||||||
chr4:99538605
|
T | C | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.629-558T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538605 | ||||||
chr4:99538698
|
A | G | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.629-465A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538698 | ||||||
chr4:99538709
|
A | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(162): Show | 182 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.629-454A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 6/8 | chr4 | 99538709 | ||||||
chr4:99539374
|
A | G | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
splice_region_variant&intron_variant | LOW | c.836+4A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539374 | ||||||
chr4:99539396
|
A | C | 1 | a0004c0005t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.836+26A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539396 | ||||||
chr4:99539681
|
T | C | 3 | a0002c0004t0001g0033a0002c0004t0001g0034a0002c0004t0001g0035 | 3 | HG00639.hp2 HG01257.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.836+311T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539681 | ||||||
chr4:99539854
|
C | T | 1 | a0002c0004t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.836+484C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539854 | ||||||
chr4:99539867
|
A | C | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.836+497A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99539867 | ||||||
chr4:99540010
|
T | A | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.837-402T>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99540010 | ||||||
chr4:99540065
|
A | G | 1 | a0003c0002t0001g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837-347A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99540065 | ||||||
chr4:99540114
|
A | G | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.837-298A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 7/8 | chr4 | 99540114 | ||||||
chr4:99540553
|
A | C | 1 | a0004c0005t0001g0246 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.880+98A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540553 | ||||||
chr4:99540712
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(59): Show | 71 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.880+257G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540712 | ||||||
chr4:99540875
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.880+420G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540875 | ||||||
chr4:99540900
|
A | C | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880+445A>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540900 | ||||||
chr4:99540928
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0108a0001c0001t0001g0111others(5): Show | 9 | HG00639.hp1 HG00733.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.880+473C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540928 | ||||||
chr4:99540980
|
A | G | 81 | a0001c0001t0001g0015a0001c0001t0001g0068a0001c0001t0001g0108others(78): Show | 88 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.880+525A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99540980 | ||||||
chr4:99541235
|
C | T | 1 | a0004c0005t0001g0054 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.881-675C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541235 | ||||||
chr4:99541262
|
T | C | 8 | a0005c0006t0001g0029a0005c0006t0001g0270a0005c0006t0001g0271others(5): Show | 9 | HG01975.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.881-648T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541262 | ||||||
chr4:99541277
|
A | G | 3 | a0003c0008t0001g0091a0003c0008t0001g0092a0003c0008t0001g0093 | 3 | HG02615.hp2 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.881-633A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541277 | ||||||
chr4:99541451
|
A | G | 1 | a0002c0003t0001g0324 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.881-459A>G | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541451 | ||||||
chr4:99541537
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0088others(60): Show | 72 | HG00558.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.881-373T>C | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541537 | ||||||
chr4:99541566
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0018others(141): Show | 160 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.881-344C>T | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541566 | ||||||
chr4:99541764
|
G | A | 1 | a0002c0004t0001g0033 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.881-146G>A | C4orf17 | ENSG00000138813.10 | transcript | ENST00000326581.9 | protein_coding | 8/8 | chr4 | 99541764 |