geneid | 1271 |
---|---|
ensemblid | ENSG00000122756.15 |
hgncid | 2170 |
symbol | CNTFR |
name | ciliary neurotrophic factor receptor |
refseq_nuc | NM_147164.3 |
refseq_prot | NP_671693.1 |
ensembl_nuc | ENST00000378980.8 |
ensembl_prot | ENSP00000368265.3 |
mane_status | MANE Select |
chr | chr9 |
start | 34551433 |
end | 34589724 |
strand | - |
ver | v1.2 |
region | chr9:34551433-34589724 |
region5000 | chr9:34546433-34594724 |
regionname0 | CNTFR_chr9_34551433_34589724 |
regionname5000 | CNTFR_chr9_34546433_34594724 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 373 | 400 | 95 | 82 | 164 | 14 | 43 | 126 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0002 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0003 | 0/0 | 373 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1208 | 377 | 93 | 79 | 149 | 14 | 40 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0002 | 0/0 | 1208 | 13 | 0 | 1 | 12 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0003 | 0/0 | 1208 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0004 | 0/0 | 1208 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0005 | 0/0 | 1208 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0006 | 0/0 | 1208 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0007 | 0/0 | 1208 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0008 | 0/0 | 1208 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0009 | 0/0 | 1208 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0010 | 0/0 | 1208 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
c0011 | 0/0 | 1208 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 920 | 268 | 71 | 54 | 99 | 14 | 28 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0002 | 0/0 | 920 | 87 | 13 | 6 | 58 | 0 | 10 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0003 | 0/0 | 920 | 31 | 2 | 19 | 5 | 0 | 5 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0004 | 0/0 | 920 | 8 | 7 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0005 | 0/0 | 920 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0006 | 0/0 | 920 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0007 | 0/0 | 920 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0008 | 0/0 | 920 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
t0009 | 0/0 | 920 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 0 | 8 | 1 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0002 | 0/0 | 11 | 1 | 6 | 0 | 1 | 3 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0003 | 0/0 | 7 | 3 | 4 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0005 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0008 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0010 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1208 | 377 | 93 | 79 | 149 | 14 | 40 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0002 | 0/0 | 1208 | 13 | 0 | 1 | 12 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0003 | 0/0 | 1208 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0004 | 0/0 | 1208 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0005 | 0/0 | 1208 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0008 | 0/0 | 1208 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0009 | 0/0 | 1208 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0010 | 0/0 | 1208 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0011 | 0/0 | 1208 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0002c0006 | 0/0 | 1208 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0003c0007 | 0/0 | 1208 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2127 | 258 | 68 | 53 | 96 | 14 | 25 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0002 | 0/0 | 2127 | 73 | 13 | 4 | 46 | 0 | 10 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0003 | 0/0 | 2127 | 30 | 2 | 19 | 5 | 0 | 4 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0004 | 0/0 | 2127 | 8 | 7 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0005 | 0/0 | 2127 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0006 | 0/0 | 2127 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0007 | 0/0 | 2127 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0008 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0001t0009 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0002t0002 | 0/0 | 2127 | 13 | 0 | 1 | 12 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0003t0001 | 0/0 | 2127 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0004t0001 | 0/0 | 2127 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0005t0001 | 0/0 | 2127 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0008t0003 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0009t0002 | 0/0 | 2127 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0010t0001 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0001c0011t0001 | 0/0 | 2127 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0002c0006t0001 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
a0003c0007t0001 | 0/0 | 2127 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | copy fasta | chr9 | 34546433 | 34594724 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 8 | 1 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0002 | 0/0 | 11 | 1 | 6 | 0 | 1 | 3 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0003 | 0/0 | 7 | 3 | 4 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0010 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0005 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0004g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0004g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0006g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0003t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0004t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0008t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0009t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0010t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0001c0011t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0002c0006t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
a0003c0007t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01074 | hp1 | a0001 | c0009 | t0002 | g0265 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0282 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CDX | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02698 | hp1 | a0001 | c0005 | t0001 | g0247 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02723 | hp1 | a0002 | c0006 | t0001 | g0225 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02738 | hp1 | a0001 | c0005 | t0001 | g0093 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0045 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03491 | hp1 | a0001 | c0008 | t0003 | g0260 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0256 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03654 | hp1 | a0003 | c0007 | t0001 | g0223 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | STU | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | CHB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0041 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18993 | hp1 | a0001 | c0004 | t0001 | g0041 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19000 | hp2 | a0001 | c0011 | t0001 | g0277 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19089 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ASW | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | GIH | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG02559 | hp2 | a0001 | c0010 | t0001 | g0061 | AFR | ACB | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0211 | REF | REF | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0167 | REF | REF | CNTFR_chr9_34546433_34594724 | CNTFR | chr9 | 34546433 | 34594724 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34564643
|
C | T | 1 | a0003 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.275G>A | p.Arg92His | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 556/2038 | 275/1119 | 92/372 | chr9 | 34564643 | ||
chr9:34564745
|
C | T | 1 | a0002 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.173G>A | p.Arg58Gln | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 454/2038 | 173/1119 | 58/372 | chr9 | 34564745 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34556348
|
C | T | 1 | a0001c0008 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.675G>A | p.Thr225Thr | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/10 | 956/2038 | 675/1119 | 225/372 | chr9 | 34556348 | ||
chr9:34556393
|
C | T | 1 | a0001c0003 | 2 | HG01243.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.630G>A | p.Val210Val | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/10 | 911/2038 | 630/1119 | 210/372 | chr9 | 34556393 | ||
chr9:34557905
|
G | A | 1 | a0001c0002 | 13 | HG00558.hp2 HG00642.hp2 HG02074.hp1 others(10): Show |
synonymous_variant | LOW | c.399C>T | p.Thr133Thr | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 5/10 | 680/2038 | 399/1119 | 133/372 | chr9 | 34557905 | ||
chr9:34564723
|
G | C | 1 | a0001c0009 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.195C>G | p.Ala65Ala | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 476/2038 | 195/1119 | 65/372 | chr9 | 34564723 | ||
chr9:34564813
|
G | A | 1 | a0001c0005 | 2 | HG02698.hp1 HG02738.hp1 |
synonymous_variant | LOW | c.105C>T | p.Tyr35Tyr | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/10 | 386/2038 | 105/1119 | 35/372 | chr9 | 34564813 | ||
chr9:34568928
|
T | G | 1 | a0001c0010 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.54A>C | p.Ala18Ala | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/10 | 335/2038 | 54/1119 | 18/372 | chr9 | 34568928 | ||
chr9:34568937
|
G | A | 1 | a0001c0011 | 1 | NA19000.hp2 | synonymous_variant | LOW | c.45C>T | p.Ala15Ala | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/10 | 326/2038 | 45/1119 | 15/372 | chr9 | 34568937 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34551448
|
G | A | 1 | a0001c0001t0006 | 2 | HG01106.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*623C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 623 | chr9 | 34551448 | |||||
chr9:34551762
|
C | T | 1 | a0001c0001t0008 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 309 | chr9 | 34551762 | |||||
chr9:34551898
|
G | A | 3 | a0001c0001t0002a0001c0002t0002a0001c0009t0002 | 87 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*173C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 173 | chr9 | 34551898 | |||||
chr9:34551921
|
C | T | 1 | a0001c0001t0009 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 150 | chr9 | 34551921 | |||||
chr9:34551922
|
G | A | 1 | a0001c0001t0007 | 2 | HG02258.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 149 | chr9 | 34551922 | |||||
chr9:34551931
|
G | A | 1 | a0001c0001t0009 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 140 | chr9 | 34551931 | |||||
chr9:34552020
|
G | C | 2 | a0001c0001t0003a0001c0008t0003 | 31 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*51C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 10/10 | 51 | chr9 | 34552020 | |||||
chr9:34589563
|
C | T | 1 | a0001c0001t0005 | 2 | NA18946.hp1 NA19089.hp2 |
5_prime_UTR_variant | MODIFIER | c.-120G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/10 | 20582 | chr9 | 34589563 | |||||
chr9:34589662
|
G | C | 1 | a0001c0001t0004 | 8 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-219C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/10 | 20681 | chr9 | 34589662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:34552075
|
T | C | 1 | a0001c0004t0001g0041 | 2 | NA18973.hp2 NA18993.hp1 |
splice_region_variant&intron_variant | LOW | c.1119-4A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 9/9 | chr9 | 34552075 | ||||||
chr9:34552368
|
T | TG | 8 | a0001c0001t0001g0028a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 9 | HG02647.hp2 HG02965.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-40dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552368 | ||||||
chr9:34552383
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.950-54A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552383 | ||||||
chr9:34552439
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.950-110G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552439 | ||||||
chr9:34552660
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.949+14C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 8/9 | chr9 | 34552660 | ||||||
chr9:34552913
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.769-59G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34552913 | ||||||
chr9:34553219
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.769-365C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553219 | ||||||
chr9:34553279
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.769-425G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553279 | ||||||
chr9:34553413
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769-559A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553413 | ||||||
chr9:34553613
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0108 | 3 | HG02486.hp1 HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.769-759C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553613 | ||||||
chr9:34553650
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0186a0001c0001t0001g0254others(1): Show | 8 | HG00280.hp2 HG00735.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.769-796C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553650 | ||||||
chr9:34553669
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.769-815A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553669 | ||||||
chr9:34553940
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 307 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.769-1086C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553940 | ||||||
chr9:34553970
|
G | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.769-1116C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34553970 | ||||||
chr9:34554002
|
G | A | 23 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.769-1148C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554002 | ||||||
chr9:34554015
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0177 | 5 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.769-1161C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554015 | ||||||
chr9:34554017
|
G | A | 1 | a0001c0001t0003g0249 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.769-1163C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554017 | ||||||
chr9:34554022
|
G | A | 1 | a0001c0001t0007g0088 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.769-1168C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554022 | ||||||
chr9:34554040
|
G | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 307 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.769-1186C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554040 | ||||||
chr9:34554062
|
G | A | 23 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.769-1208C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554062 | ||||||
chr9:34554146
|
C | T | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp1 HG02735.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-1292G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554146 | ||||||
chr9:34554156
|
C | A | 5 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0069others(2): Show | 7 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.769-1302G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554156 | ||||||
chr9:34554229
|
G | C | 25 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0155others(22): Show | 36 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.769-1375C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554229 | ||||||
chr9:34554261
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.769-1407G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554261 | ||||||
chr9:34554335
|
G | A | 1 | a0001c0001t0003g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.769-1481C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554335 | ||||||
chr9:34554355
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.769-1501T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554355 | ||||||
chr9:34554426
|
G | A | 1 | a0001c0001t0009g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.769-1572C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554426 | ||||||
chr9:34554471
|
T | A | 1 | a0001c0001t0001g0044 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.769-1617A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554471 | ||||||
chr9:34554603
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0003g0049 | 3 | HG02622.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.768+1652G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554603 | ||||||
chr9:34554636
|
A | G | 25 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0155others(22): Show | 36 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.768+1619T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554636 | ||||||
chr9:34554718
|
C | T | 23 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+1537G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554718 | ||||||
chr9:34554737
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.768+1518A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554737 | ||||||
chr9:34554893
|
G | C | 6 | a0001c0001t0001g0086a0001c0001t0004g0026a0001c0001t0004g0055others(3): Show | 9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.768+1362C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554893 | ||||||
chr9:34554941
|
C | T | 1 | a0001c0001t0001g0015 | 3 | HG02647.hp1 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.768+1314G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34554941 | ||||||
chr9:34555001
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 307 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.768+1254A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555001 | ||||||
chr9:34555028
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0160 | 2 | HG01891.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.768+1227G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555028 | ||||||
chr9:34555108
|
C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0034others(8): Show | 16 | HG01496.hp1 HG02109.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.768+1147G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555108 | ||||||
chr9:34555334
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.768+921C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555334 | ||||||
chr9:34555447
|
T | C | 23 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+808A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555447 | ||||||
chr9:34555464
|
G | A | 1 | a0003c0007t0001g0223 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.768+791C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555464 | ||||||
chr9:34555483
|
C | T | 23 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+772G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555483 | ||||||
chr9:34555502
|
G | C | 23 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.768+753C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555502 | ||||||
chr9:34555818
|
T | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(32): Show | 48 | HG00639.hp2 HG00738.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.768+437A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555818 | ||||||
chr9:34555883
|
G | GCCCGCCA others(9): Show |
1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.768+356_768+371dup others(16): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555883 | ||||||
chr9:34555903
|
GCCATCTC others(41): Show |
G | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.768+304_768+351del others(48): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555903 | ||||||
chr9:34555918
|
T | C | 22 | a0001c0001t0001g0160a0001c0001t0001g0259a0001c0001t0003g0005others(19): Show | 33 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.768+337A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555918 | ||||||
chr9:34555933
|
C | T | 22 | a0001c0001t0001g0160a0001c0001t0001g0259a0001c0001t0003g0005others(19): Show | 33 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.768+322G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555933 | ||||||
chr9:34555935
|
G | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0231 | 2 | HG01891.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.768+320C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555935 | ||||||
chr9:34555935
|
GCCATCTC others(9): Show |
G | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.768+304_768+319del others(16): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555935 | ||||||
chr9:34555963
|
C | CCCCGCCA others(13): Show |
3 | a0001c0001t0001g0071a0001c0001t0001g0139a0001c0001t0009g0256 | 3 | HG01891.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.768+272_768+291dup others(20): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555963 | ||||||
chr9:34555973
|
T | G | 1 | a0001c0001t0001g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.768+282A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34555973 | ||||||
chr9:34556024
|
C | G | 27 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(24): Show | 39 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.768+231G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34556024 | ||||||
chr9:34556049
|
C | A | 1 | a0001c0001t0001g0190 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.768+206G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34556049 | ||||||
chr9:34556194
|
C | CCACTCAC others(15): Show |
14 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(11): Show | 24 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.768+39_768+60dupTT others(20): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 7/9 | chr9 | 34556194 | ||||||
chr9:34556455
|
A | T | 27 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(24): Show | 39 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.605-37T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556455 | ||||||
chr9:34556795
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.605-377G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556795 | ||||||
chr9:34556844
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.605-426T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556844 | ||||||
chr9:34556935
|
C | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.605-517G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34556935 | ||||||
chr9:34557073
|
G | A | 4 | a0001c0001t0002g0127a0001c0001t0002g0142a0001c0001t0002g0143others(1): Show | 4 | HG00609.hp2 NA18970.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.604+453C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557073 | ||||||
chr9:34557099
|
T | TG | 72 | a0001c0001t0001g0034a0001c0001t0001g0121a0001c0001t0001g0137others(69): Show | 95 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.604+426dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557099 | ||||||
chr9:34557122
|
G | A | 1 | a0001c0001t0001g0044 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.604+404C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557122 | ||||||
chr9:34557141
|
C | T | 2 | a0001c0002t0002g0131a0001c0002t0002g0237 | 2 | NA19066.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.604+385G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557141 | ||||||
chr9:34557192
|
T | TG | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.604+333dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557192 | ||||||
chr9:34557194
|
G | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG01891.hp1 HG02965.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+332C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557194 | ||||||
chr9:34557249
|
C | G | 1 | a0001c0001t0001g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.604+277G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557249 | ||||||
chr9:34557314
|
C | T | 1 | a0001c0001t0002g0138 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.604+212G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557314 | ||||||
chr9:34557315
|
G | A | 28 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(25): Show | 39 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.604+211C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557315 | ||||||
chr9:34557392
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.604+134G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 6/9 | chr9 | 34557392 | ||||||
chr9:34557817
|
G | A | 1 | a0001c0001t0004g0281 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.437+50C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 5/9 | chr9 | 34557817 | ||||||
chr9:34558080
|
C | G | 1 | a0001c0001t0001g0187 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.320-96G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558080 | ||||||
chr9:34558235
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.320-251G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558235 | ||||||
chr9:34558518
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-534C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558518 | ||||||
chr9:34558576
|
T | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.320-592A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558576 | ||||||
chr9:34558644
|
A | G | 24 | a0001c0001t0001g0064a0001c0001t0001g0160a0001c0001t0001g0213others(21): Show | 35 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.320-660T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558644 | ||||||
chr9:34558667
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.320-683T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558667 | ||||||
chr9:34558751
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320-767A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558751 | ||||||
chr9:34558913
|
C | T | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 7 | HG01891.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-929G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558913 | ||||||
chr9:34558914
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0243a0001c0001t0002g0244others(1): Show | 4 | HG00597.hp2 NA18949.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-930C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34558914 | ||||||
chr9:34559031
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.320-1047G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559031 | ||||||
chr9:34559092
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.320-1108G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559092 | ||||||
chr9:34559100
|
G | A | 5 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp1 HG02735.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-1116C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559100 | ||||||
chr9:34559503
|
T | C | 154 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(151): Show | 211 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(208): Show |
intron_variant | MODIFIER | c.320-1519A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559503 | ||||||
chr9:34559503
|
T | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1519A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559503 | ||||||
chr9:34559524
|
C | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1540G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559524 | ||||||
chr9:34559563
|
T | C | 24 | a0001c0001t0001g0064a0001c0001t0001g0097a0001c0001t0001g0098others(21): Show | 35 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.320-1579A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559563 | ||||||
chr9:34559614
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111 | 4 | HG03516.hp1 NA18522.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-1630G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559614 | ||||||
chr9:34559835
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.320-1851G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559835 | ||||||
chr9:34559888
|
T | A | 6 | a0001c0001t0001g0086a0001c0001t0004g0026a0001c0001t0004g0055others(3): Show | 9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.320-1904A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559888 | ||||||
chr9:34559914
|
C | G | 23 | a0001c0001t0001g0064a0001c0001t0001g0160a0001c0001t0001g0259others(20): Show | 34 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.320-1930G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559914 | ||||||
chr9:34559918
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.320-1934T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559918 | ||||||
chr9:34559924
|
C | T | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0022others(16): Show | 29 | HG02083.hp1 HG02132.hp2 HG02523.hp2 others(26): Show |
intron_variant | MODIFIER | c.320-1940G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34559924 | ||||||
chr9:34560275
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0116 | 3 | NA18946.hp2 NA18988.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.320-2291G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560275 | ||||||
chr9:34560322
|
G | A | 90 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(87): Show | 124 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.320-2338C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560322 | ||||||
chr9:34560351
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.320-2367C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560351 | ||||||
chr9:34560544
|
G | A | 10 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0063others(7): Show | 14 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.320-2560C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560544 | ||||||
chr9:34560605
|
A | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-2621T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560605 | ||||||
chr9:34560620
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0273others(3): Show | 13 | NA18941.hp2 NA18942.hp1 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.320-2636C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560620 | ||||||
chr9:34560647
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.320-2663A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560647 | ||||||
chr9:34560715
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-2731G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560715 | ||||||
chr9:34560737
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.320-2753C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560737 | ||||||
chr9:34560798
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.320-2814G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560798 | ||||||
chr9:34560827
|
G | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0052others(6): Show | 15 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.320-2843C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560827 | ||||||
chr9:34560981
|
C | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.320-2997G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34560981 | ||||||
chr9:34561069
|
C | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(26): Show | 39 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(36): Show |
intron_variant | MODIFIER | c.320-3085G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561069 | ||||||
chr9:34561162
|
G | A | 70 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(67): Show | 94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.320-3178C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561162 | ||||||
chr9:34561250
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(13): Show | 26 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.320-3266G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561250 | ||||||
chr9:34561341
|
G | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG02615.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+3258C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561341 | ||||||
chr9:34561470
|
T | C | 33 | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0064others(30): Show | 46 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.319+3129A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561470 | ||||||
chr9:34561531
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.319+3068C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561531 | ||||||
chr9:34561562
|
T | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.319+3037A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561562 | ||||||
chr9:34561744
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.319+2855C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561744 | ||||||
chr9:34561810
|
C | T | 70 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(67): Show | 94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.319+2789G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561810 | ||||||
chr9:34561885
|
A | C | 1 | a0001c0001t0002g0134 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.319+2714T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34561885 | ||||||
chr9:34562095
|
A | G | 30 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(27): Show | 41 | HG00544.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.319+2504T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562095 | ||||||
chr9:34562127
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+2472G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562127 | ||||||
chr9:34562193
|
T | C | 1 | a0001c0001t0002g0150 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.319+2406A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562193 | ||||||
chr9:34562212
|
A | G | 2 | a0001c0001t0006g0045a0001c0001t0009g0256 | 3 | HG01106.hp1 HG03239.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.319+2387T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562212 | ||||||
chr9:34562268
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.319+2331C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562268 | ||||||
chr9:34562269
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319+2330G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562269 | ||||||
chr9:34562350
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.319+2249C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562350 | ||||||
chr9:34562501
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.319+2098G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562501 | ||||||
chr9:34562588
|
G | A | 1 | a0001c0001t0003g0049 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.319+2011C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562588 | ||||||
chr9:34562592
|
C | G | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(53): Show | 77 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.319+2007G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562592 | ||||||
chr9:34562639
|
C | T | 1 | a0001c0010t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.319+1960G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562639 | ||||||
chr9:34562816
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.319+1783G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562816 | ||||||
chr9:34562833
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG02965.hp1 HG03516.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+1766G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562833 | ||||||
chr9:34562915
|
T | C | 1 | a0001c0001t0001g0039 | 2 | NA18959.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.319+1684A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34562915 | ||||||
chr9:34563172
|
G | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(3): Show | 7 | HG01891.hp1 HG02965.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1427C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563172 | ||||||
chr9:34563235
|
C | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0228 | 3 | HG01255.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.319+1364G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563235 | ||||||
chr9:34563301
|
GTGCTGGG others(15): Show |
G | 1 | a0001c0001t0002g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.319+1276_319+1297d others(24): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563301 | ||||||
chr9:34563321
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.319+1278G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563321 | ||||||
chr9:34563466
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.319+1133C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563466 | ||||||
chr9:34563565
|
A | G | 28 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0073others(25): Show | 39 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.319+1034T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563565 | ||||||
chr9:34563657
|
C | A | 2 | a0001c0001t0003g0074a0001c0001t0003g0087 | 2 | HG01167.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.319+942G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563657 | ||||||
chr9:34563657
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0269 | 2 | HG01928.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.319+942G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563657 | ||||||
chr9:34563727
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.319+872G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563727 | ||||||
chr9:34563758
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0137 | 2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.319+841C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563758 | ||||||
chr9:34563760
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.319+839G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563760 | ||||||
chr9:34563830
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.319+769A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563830 | ||||||
chr9:34563868
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.319+731A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34563868 | ||||||
chr9:34564027
|
G | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.319+572C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564027 | ||||||
chr9:34564117
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.319+482C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564117 | ||||||
chr9:34564181
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+418G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564181 | ||||||
chr9:34564276
|
G | A | 70 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(67): Show | 94 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.319+323C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564276 | ||||||
chr9:34564394
|
G | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+205C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 4/9 | chr9 | 34564394 | ||||||
chr9:34564842
|
G | A | 1 | a0001c0001t0003g0051 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.86-10C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564842 | ||||||
chr9:34564848
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.86-16C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564848 | ||||||
chr9:34564895
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(11): Show | 24 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.86-63G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564895 | ||||||
chr9:34564940
|
G | T | 1 | a0001c0001t0003g0249 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.86-108C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34564940 | ||||||
chr9:34565082
|
C | T | 19 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(16): Show | 29 | HG00733.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-250G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565082 | ||||||
chr9:34565083
|
G | C | 7 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-251C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565083 | ||||||
chr9:34565096
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0137 | 2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.86-264A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565096 | ||||||
chr9:34565134
|
A | T | 1 | a0001c0001t0002g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.86-302T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565134 | ||||||
chr9:34565212
|
G | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(2): Show | 6 | HG02965.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-380C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565212 | ||||||
chr9:34565298
|
A | T | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-466T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565298 | ||||||
chr9:34565300
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-468A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565300 | ||||||
chr9:34565301
|
C | A | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-469G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565301 | ||||||
chr9:34565302
|
C | G | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-470G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565302 | ||||||
chr9:34565303
|
T | G | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-471A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565303 | ||||||
chr9:34565304
|
T | A | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-472A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565304 | ||||||
chr9:34565305
|
T | G | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-473A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565305 | ||||||
chr9:34565307
|
T | C | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-475A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565307 | ||||||
chr9:34565308
|
C | G | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-476G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565308 | ||||||
chr9:34565311
|
T | G | 1 | a0001c0001t0002g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.86-479A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565311 | ||||||
chr9:34565367
|
AC | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-536delG | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565367 | ||||||
chr9:34565445
|
G | A | 1 | a0001c0010t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.86-613C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565445 | ||||||
chr9:34565572
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-740C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565572 | ||||||
chr9:34565783
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.86-951T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565783 | ||||||
chr9:34565935
|
A | G | 1 | a0001c0001t0002g0123 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.86-1103T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565935 | ||||||
chr9:34565981
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.86-1149G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34565981 | ||||||
chr9:34566030
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-1198A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566030 | ||||||
chr9:34566152
|
C | CT | 4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0111others(1): Show | 5 | HG03516.hp1 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-1321dupA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566152 | ||||||
chr9:34566192
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.86-1360T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566192 | ||||||
chr9:34566226
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0003t0001g0036 | 4 | HG01243.hp1 HG03098.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-1394C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566226 | ||||||
chr9:34566231
|
C | T | 1 | a0001c0001t0001g0044 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.86-1399G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566231 | ||||||
chr9:34566259
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.86-1427C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566259 | ||||||
chr9:34566619
|
A | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(8): Show | 21 | HG02056.hp2 HG02523.hp1 NA18941.hp2 others(18): Show |
intron_variant | MODIFIER | c.86-1787T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566619 | ||||||
chr9:34566729
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0173a0001c0001t0001g0175others(2): Show | 8 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-1897G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566729 | ||||||
chr9:34566736
|
G | A | 157 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(154): Show | 216 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(213): Show |
intron_variant | MODIFIER | c.86-1904C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566736 | ||||||
chr9:34566744
|
A | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0069a0001c0001t0001g0084others(2): Show | 6 | HG00639.hp2 HG00738.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-1912T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566744 | ||||||
chr9:34566801
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.86-1969C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566801 | ||||||
chr9:34566884
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG02615.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+2013G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566884 | ||||||
chr9:34566971
|
G | A | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.85+1926C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34566971 | ||||||
chr9:34567050
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG02258.hp1 HG02738.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1847G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567050 | ||||||
chr9:34567182
|
AT | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.85+1714delA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567182 | ||||||
chr9:34567202
|
A | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 380 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(377): Show |
intron_variant | MODIFIER | c.85+1695T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567202 | ||||||
chr9:34567422
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.85+1475T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567422 | ||||||
chr9:34567542
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.85+1355G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567542 | ||||||
chr9:34567670
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.85+1227C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567670 | ||||||
chr9:34567748
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG02258.hp1 HG02738.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1149G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567748 | ||||||
chr9:34567849
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0111 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.85+1048C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34567849 | ||||||
chr9:34568008
|
C | A | 1 | a0001c0001t0007g0088 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+889G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568008 | ||||||
chr9:34568340
|
A | G | 2 | a0001c0001t0002g0090a0001c0005t0001g0093 | 2 | HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.85+557T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568340 | ||||||
chr9:34568497
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+400A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568497 | ||||||
chr9:34568570
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0139 | 3 | HG01891.hp2 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.85+327G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568570 | ||||||
chr9:34568742
|
A | G | 1 | a0001c0010t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85+155T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568742 | ||||||
chr9:34568859
|
G | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+38C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568859 | ||||||
chr9:34568869
|
T | C | 1 | a0001c0010t0001g0061 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85+28A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 3/9 | chr9 | 34568869 | ||||||
chr9:34568995
|
C | A | 1 | a0001c0001t0003g0249 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1-14G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34568995 | ||||||
chr9:34569012
|
T | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 378 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(375): Show |
intron_variant | MODIFIER | c.1-31A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569012 | ||||||
chr9:34569124
|
C | T | 6 | a0001c0001t0001g0086a0001c0001t0004g0026a0001c0001t0004g0055others(3): Show | 9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1-143G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569124 | ||||||
chr9:34569299
|
T | C | 69 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(66): Show | 93 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1-318A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569299 | ||||||
chr9:34569473
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1-492C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569473 | ||||||
chr9:34569496
|
G | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-515C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569496 | ||||||
chr9:34569668
|
G | T | 1 | a0001c0001t0002g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1-687C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569668 | ||||||
chr9:34569669
|
T | G | 1 | a0001c0001t0002g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1-688A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569669 | ||||||
chr9:34569670
|
G | T | 1 | a0001c0001t0002g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1-689C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569670 | ||||||
chr9:34569679
|
C | A | 1 | a0001c0001t0002g0134 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1-698G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569679 | ||||||
chr9:34569701
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(46): Show | 63 | HG00639.hp2 HG00738.hp2 HG01175.hp2 others(60): Show |
intron_variant | MODIFIER | c.1-720G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569701 | ||||||
chr9:34569963
|
C | G | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-982G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34569963 | ||||||
chr9:34570352
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1-1371G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570352 | ||||||
chr9:34570356
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 380 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(377): Show |
intron_variant | MODIFIER | c.1-1375G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570356 | ||||||
chr9:34570442
|
C | T | 4 | a0001c0001t0001g0185a0001c0001t0002g0076a0001c0001t0002g0077others(1): Show | 4 | HG00280.hp1 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-1461G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570442 | ||||||
chr9:34570533
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0063others(6): Show | 13 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-1552G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570533 | ||||||
chr9:34570574
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0111 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1-1593C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570574 | ||||||
chr9:34570747
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.1-1766A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570747 | ||||||
chr9:34570836
|
G | C | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 10 | HG01074.hp1 HG01496.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1-1855C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570836 | ||||||
chr9:34570856
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.1-1875T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570856 | ||||||
chr9:34570863
|
T | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0137 | 2 | HG01109.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1-1882A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570863 | ||||||
chr9:34570990
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1-2009G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570990 | ||||||
chr9:34570992
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(63): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1-2011G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570992 | ||||||
chr9:34570993
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1-2012G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34570993 | ||||||
chr9:34571015
|
T | G | 7 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 9 | HG01074.hp1 HG01496.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-2034A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571015 | ||||||
chr9:34571176
|
C | T | 1 | a0001c0001t0003g0049 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1-2195G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571176 | ||||||
chr9:34571437
|
T | C | 66 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(63): Show | 84 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(81): Show |
intron_variant | MODIFIER | c.1-2456A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571437 | ||||||
chr9:34571465
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(13): Show | 26 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-2484A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571465 | ||||||
chr9:34571546
|
G | A | 6 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(3): Show | 7 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.1-2565C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571546 | ||||||
chr9:34571553
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1-2572G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571553 | ||||||
chr9:34571558
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0191 | 2 | HG03540.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1-2577C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571558 | ||||||
chr9:34571559
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1-2578G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571559 | ||||||
chr9:34571561
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1-2580A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
T | TAC | 51 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0025others(48): Show | 73 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.1-2582_1-2581dupGT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
T | TACAC | 9 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0050others(6): Show | 12 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1-2584_1-2581dupGT others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
T | TACACAC | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0052others(26): Show | 48 | HG00544.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1-2586_1-2581dupGT others(4): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
T | TACACACA others(1): Show |
3 | a0001c0001t0001g0241a0001c0001t0002g0126a0001c0001t0003g0094 | 3 | HG00741.hp2 HG01192.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1-2588_1-2581dupGT others(6): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0273 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1-2590_1-2581dupGT others(8): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
TAC | T | 37 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0104others(34): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1-2582_1-2581delGT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
TACAC | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0063others(6): Show | 13 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-2584_1-2581delGT others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0081 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1-2590_1-2581delGT others(8): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571561
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1-2592_1-2581delGT others(10): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571561 | ||||||
chr9:34571588
|
A | T | 1 | a0001c0001t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1-2607T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571588 | ||||||
chr9:34571602
|
G | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(13): Show | 21 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1-2621C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571602 | ||||||
chr9:34571644
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0168 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1-2663G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571644 | ||||||
chr9:34571665
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-2684G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571665 | ||||||
chr9:34571680
|
C | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0110 | 3 | HG02895.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-2699G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571680 | ||||||
chr9:34571747
|
A | T | 4 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1-2766T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571747 | ||||||
chr9:34571753
|
A | G | 1 | a0001c0001t0003g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1-2772T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571753 | ||||||
chr9:34571800
|
A | G | 16 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0027others(13): Show | 21 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1-2819T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571800 | ||||||
chr9:34571815
|
G | A | 9 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0063others(6): Show | 13 | HG01496.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-2834C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571815 | ||||||
chr9:34571868
|
T | C | 1 | a0001c0002t0002g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1-2887A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571868 | ||||||
chr9:34571964
|
G | C | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-2983C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34571964 | ||||||
chr9:34572151
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1-3170G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572151 | ||||||
chr9:34572216
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0092others(3): Show | 6 | HG02258.hp1 HG02738.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1-3235G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572216 | ||||||
chr9:34572373
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1-3392G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572373 | ||||||
chr9:34572396
|
G | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.1-3415C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572396 | ||||||
chr9:34572450
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1-3469T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572450 | ||||||
chr9:34572687
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1-3706C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572687 | ||||||
chr9:34572769
|
T | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1-3788A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572769 | ||||||
chr9:34572817
|
C | T | 67 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(64): Show | 91 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1-3836G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572817 | ||||||
chr9:34572827
|
G | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1-3846C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572827 | ||||||
chr9:34572909
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1-3928C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572909 | ||||||
chr9:34572922
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1-3941C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572922 | ||||||
chr9:34572927
|
C | T | 1 | a0001c0001t0009g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1-3946G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572927 | ||||||
chr9:34572931
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1-3950T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572931 | ||||||
chr9:34572993
|
C | T | 7 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(4): Show | 8 | HG00099.hp1 HG01070.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1-4012G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34572993 | ||||||
chr9:34573032
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1-4051C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573032 | ||||||
chr9:34573146
|
CG | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 394 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(391): Show |
intron_variant | MODIFIER | c.1-4166delC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573146 | ||||||
chr9:34573286
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1-4305T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573286 | ||||||
chr9:34573330
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1-4349A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573330 | ||||||
chr9:34573336
|
C | T | 1 | a0001c0001t0001g0054 | 2 | NA18947.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1-4355G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573336 | ||||||
chr9:34573472
|
A | T | 1 | a0001c0001t0001g0183 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1-4491T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573472 | ||||||
chr9:34573596
|
G | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0052others(29): Show | 49 | HG00544.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1-4615C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573596 | ||||||
chr9:34573608
|
C | G | 1 | a0001c0001t0003g0049 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1-4627G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573608 | ||||||
chr9:34573814
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1-4833G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573814 | ||||||
chr9:34573918
|
G | C | 1 | a0001c0001t0001g0193 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1-4937C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34573918 | ||||||
chr9:34574087
|
C | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(23): Show | 36 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(33): Show |
intron_variant | MODIFIER | c.1-5106G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574087 | ||||||
chr9:34574102
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(13): Show | 26 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-5121G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574102 | ||||||
chr9:34574103
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 6 | HG01496.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1-5122C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574103 | ||||||
chr9:34574121
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0110 | 3 | HG02895.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1-5140C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574121 | ||||||
chr9:34574141
|
G | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-5160C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574141 | ||||||
chr9:34574212
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1-5231G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574212 | ||||||
chr9:34574306
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | NA18977.hp1 NA18994.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1-5325C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574306 | ||||||
chr9:34574568
|
A | G | 2 | a0001c0001t0002g0030a0001c0001t0002g0118 | 3 | NA19060.hp2 NA19077.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1-5587T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574568 | ||||||
chr9:34574647
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1-5666C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574647 | ||||||
chr9:34574666
|
G | T | 1 | a0001c0001t0002g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1-5685C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574666 | ||||||
chr9:34574672
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1-5691A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574672 | ||||||
chr9:34574682
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1-5701G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574682 | ||||||
chr9:34574707
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1-5726G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574707 | ||||||
chr9:34574718
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1-5737A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574718 | ||||||
chr9:34574745
|
T | A | 1 | a0001c0001t0002g0138 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1-5764A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574745 | ||||||
chr9:34574765
|
C | CTG | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-5785_1-5784insCA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574765 | ||||||
chr9:34574849
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1-5868C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574849 | ||||||
chr9:34574852
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1-5871G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574852 | ||||||
chr9:34574912
|
C | T | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1-5931G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34574912 | ||||||
chr9:34575104
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-1+5991G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575104 | ||||||
chr9:34575153
|
T | A | 1 | a0001c0001t0002g0126 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-1+5942A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575153 | ||||||
chr9:34575349
|
T | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+5746A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575349 | ||||||
chr9:34575378
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0111 | 3 | HG03516.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-1+5717G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575378 | ||||||
chr9:34575516
|
G | A | 1 | a0001c0001t0003g0216 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-1+5579C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575516 | ||||||
chr9:34575524
|
T | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+5571A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575524 | ||||||
chr9:34575659
|
T | TCA | 7 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(4): Show | 7 | HG01891.hp2 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1+5434_-1+5435dup others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575659 | ||||||
chr9:34575666
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-1+5429G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575666 | ||||||
chr9:34575671
|
C | A | 5 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0139others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+5424G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575671 | ||||||
chr9:34575687
|
C | A | 1 | a0001c0001t0002g0244 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-1+5408G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575687 | ||||||
chr9:34575691
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1+5404T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575691 | ||||||
chr9:34575701
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-1+5394T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575701 | ||||||
chr9:34575812
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 392 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(389): Show |
intron_variant | MODIFIER | c.-1+5283T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575812 | ||||||
chr9:34575854
|
T | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0050others(32): Show | 53 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-1+5241A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575854 | ||||||
chr9:34575885
|
T | C | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG02615.hp2 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1+5210A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575885 | ||||||
chr9:34575987
|
G | GT | 61 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(58): Show | 85 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-1+5107dupA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34575987 | ||||||
chr9:34576076
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-1+5019G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576076 | ||||||
chr9:34576216
|
G | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG01891.hp2 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1+4879C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576216 | ||||||
chr9:34576228
|
T | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+4867A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576228 | ||||||
chr9:34576287
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-1+4808G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576287 | ||||||
chr9:34576374
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-1+4721G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576374 | ||||||
chr9:34576384
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-1+4711G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576384 | ||||||
chr9:34576456
|
A | G | 1 | a0001c0001t0003g0245 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-1+4639T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576456 | ||||||
chr9:34576467
|
G | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 59 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-1+4628C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576467 | ||||||
chr9:34576517
|
G | A | 1 | a0001c0002t0002g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-1+4578C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576517 | ||||||
chr9:34576518
|
A | G | 1 | a0001c0002t0002g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-1+4577T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576518 | ||||||
chr9:34576584
|
T | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(9): Show | 13 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1+4511A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576584 | ||||||
chr9:34576817
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-1+4278G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576817 | ||||||
chr9:34576841
|
A | T | 1 | a0001c0002t0002g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-1+4254T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576841 | ||||||
chr9:34576890
|
A | C | 62 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0121others(59): Show | 86 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-1+4205T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576890 | ||||||
chr9:34576981
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-1+4114G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34576981 | ||||||
chr9:34577130
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0002g0264others(1): Show | 4 | HG01074.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1+3965C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577130 | ||||||
chr9:34577137
|
T | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0228 | 3 | HG01255.hp1 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-1+3958A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577137 | ||||||
chr9:34577153
|
C | G | 1 | a0001c0001t0005g0057 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-1+3942G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577153 | ||||||
chr9:34577302
|
C | T | 1 | a0001c0001t0001g0211 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1+3793G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577302 | ||||||
chr9:34577383
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1+3712C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577383 | ||||||
chr9:34577413
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0234a0001c0001t0001g0235 | 6 | HG02083.hp1 HG02523.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1+3682C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577413 | ||||||
chr9:34577461
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-1+3634A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577461 | ||||||
chr9:34577531
|
G | T | 6 | a0001c0001t0001g0086a0001c0001t0004g0026a0001c0001t0004g0055others(3): Show | 9 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+3564C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577531 | ||||||
chr9:34577567
|
C | T | 5 | a0001c0001t0002g0117a0001c0001t0002g0122a0001c0001t0002g0123others(2): Show | 5 | NA18945.hp1 NA19000.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+3528G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577567 | ||||||
chr9:34577586
|
GAT | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.-1+3507_-1+3508del others(2): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577586 | ||||||
chr9:34577650
|
G | GC | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 162 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.-1+3444dupG | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577650 | ||||||
chr9:34577683
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-1+3412G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577683 | ||||||
chr9:34577715
|
C | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG02257.hp1 HG03453.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-1+3380G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577715 | ||||||
chr9:34577829
|
C | A | 13 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(10): Show | 13 | HG01891.hp2 HG02615.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1+3266G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577829 | ||||||
chr9:34577836
|
GAGAAA | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0021others(68): Show | 101 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.-1+3254_-1+3258del others(5): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577836 | ||||||
chr9:34577841
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-1+3254T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577841 | ||||||
chr9:34577894
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-1+3201T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577894 | ||||||
chr9:34577910
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-1+3185C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577910 | ||||||
chr9:34577977
|
C | CG | 7 | a0001c0001t0001g0121a0001c0001t0001g0171a0001c0001t0001g0173others(4): Show | 9 | HG00621.hp2 HG01109.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1+3117dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577977 | ||||||
chr9:34577979
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-1+3116C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577979 | ||||||
chr9:34577997
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0108 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-1+3098C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34577997 | ||||||
chr9:34578139
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0078a0001c0001t0001g0085others(5): Show | 9 | HG00738.hp1 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1+2956T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578139 | ||||||
chr9:34578162
|
C | CGGGTGGG others(10): Show |
3 | a0001c0001t0001g0109a0001c0001t0001g0241a0001c0001t0002g0240 | 3 | HG01884.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-1+2916_-1+2932dup others(17): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578162 | ||||||
chr9:34578403
|
A | G | 2 | a0001c0001t0001g0022a0001c0002t0002g0170 | 4 | NA18964.hp2 NA18980.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1+2692T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578403 | ||||||
chr9:34578555
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-1+2540A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578555 | ||||||
chr9:34578646
|
T | G | 8 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1+2449A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578646 | ||||||
chr9:34578676
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-1+2419G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578676 | ||||||
chr9:34578709
|
G | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-1+2386C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578709 | ||||||
chr9:34578800
|
T | A | 15 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(12): Show | 18 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1+2295A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578800 | ||||||
chr9:34578979
|
C | G | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1+2116G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34578979 | ||||||
chr9:34579096
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-1+1999G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579096 | ||||||
chr9:34579194
|
G | A | 8 | a0001c0001t0001g0254a0001c0001t0003g0005a0001c0001t0003g0023others(5): Show | 16 | HG00735.hp1 HG01081.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-1+1901C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579194 | ||||||
chr9:34579363
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0067a0001c0001t0001g0073others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+1732C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579363 | ||||||
chr9:34579369
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-1+1726G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579369 | ||||||
chr9:34579537
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-1+1558C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579537 | ||||||
chr9:34579847
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-1+1248A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34579847 | ||||||
chr9:34580115
|
C | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(14): Show | 27 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-1+980G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580115 | ||||||
chr9:34580259
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0034others(59): Show | 92 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-1+836C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580259 | ||||||
chr9:34580438
|
C | T | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-1+657G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580438 | ||||||
chr9:34580528
|
C | T | 68 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(65): Show | 109 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.-1+567G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580528 | ||||||
chr9:34580688
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0221 | 3 | HG02647.hp2 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-1+407G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580688 | ||||||
chr9:34580896
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.-1+199C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580896 | ||||||
chr9:34580927
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-1+168C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580927 | ||||||
chr9:34580984
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-1+111T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34580984 | ||||||
chr9:34581006
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-1+89G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 2/9 | chr9 | 34581006 | ||||||
chr9:34581524
|
C | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01891.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-111-319G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581524 | ||||||
chr9:34581527
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 23 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.-111-322G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581527 | ||||||
chr9:34581680
|
A | T | 1 | a0001c0001t0002g0118 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-111-475T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581680 | ||||||
chr9:34581821
|
A | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(93): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-111-616T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581821 | ||||||
chr9:34581864
|
C | A | 2 | a0001c0001t0007g0255a0001c0001t0009g0256 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-111-659G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34581864 | ||||||
chr9:34582091
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-111-886A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582091 | ||||||
chr9:34582276
|
C | CA | 6 | a0001c0001t0001g0052a0001c0001t0001g0064a0001c0001t0001g0258others(3): Show | 9 | HG01081.hp2 HG01346.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-111-1072dupT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 11 | HG02615.hp2 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-111-1079_-111-107 others(12): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
C | CAAAAAAA others(2): Show |
4 | a0001c0001t0001g0028a0001c0001t0001g0109a0001c0001t0001g0110others(1): Show | 7 | HG01175.hp2 HG02572.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-111-1080_-111-107 others(13): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0111a0001c0001t0004g0282 | 2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-111-1081_-111-107 others(14): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
CAA | C | 13 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(10): Show | 23 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.-111-1073_-111-107 others(6): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
CAAAA | C | 18 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(15): Show | 24 | HG00741.hp2 HG01071.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-111-1075_-111-107 others(8): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
CAAAAA | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(106): Show | 164 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-111-1076_-111-107 others(9): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582276
|
CAAAAAA | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(62): Show | 91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-111-1077_-111-107 others(10): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582276 | ||||||
chr9:34582279
|
A | C | 1 | a0001c0001t0002g0151 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-111-1074T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582279 | ||||||
chr9:34582296
|
A | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01255.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-111-1091T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582296 | ||||||
chr9:34582297
|
A | AAAAAAAA others(4): Show |
4 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG00738.hp1 HG01070.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.-111-1093_-111-109 others(15): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582297 | ||||||
chr9:34582297
|
A | AAAAAAAA others(3): Show |
9 | a0001c0001t0001g0027a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 10 | HG00099.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.-111-1093_-111-109 others(14): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582297 | ||||||
chr9:34582556
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 311 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-111-1351C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582556 | ||||||
chr9:34582601
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01891.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-111-1396C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582601 | ||||||
chr9:34582682
|
A | AG | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-111-1478dupC | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582682 | ||||||
chr9:34582851
|
G | A | 9 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(6): Show | 9 | HG00741.hp2 HG02258.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-111-1646C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582851 | ||||||
chr9:34582885
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 312 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.-111-1680A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582885 | ||||||
chr9:34582949
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 400 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(397): Show |
intron_variant | MODIFIER | c.-111-1744A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582949 | ||||||
chr9:34582952
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-111-1747C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34582952 | ||||||
chr9:34583051
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-111-1846T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583051 | ||||||
chr9:34583069
|
C | A | 21 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(18): Show | 31 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.-111-1864G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583069 | ||||||
chr9:34583120
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-111-1915G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583120 | ||||||
chr9:34583145
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 5 | HG01243.hp1 HG01891.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-111-1940G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583145 | ||||||
chr9:34583154
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-111-1949G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583154 | ||||||
chr9:34583275
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-111-2070C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583275 | ||||||
chr9:34583283
|
T | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-111-2078A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583283 | ||||||
chr9:34583479
|
G | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-111-2274C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583479 | ||||||
chr9:34583583
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(19): Show | 32 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.-111-2378G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583583 | ||||||
chr9:34583638
|
G | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(128): Show | 192 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-111-2433C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583638 | ||||||
chr9:34583799
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-111-2594C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583799 | ||||||
chr9:34583833
|
A | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0002g0116 | 3 | HG02486.hp1 HG02572.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.-111-2628T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583833 | ||||||
chr9:34583880
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-111-2675A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583880 | ||||||
chr9:34583964
|
A | G | 66 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(63): Show | 88 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-111-2759T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34583964 | ||||||
chr9:34584016
|
A | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0052others(32): Show | 52 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-111-2811T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584016 | ||||||
chr9:34584016
|
A | G | 31 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0073others(28): Show | 36 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-111-2811T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584016 | ||||||
chr9:34584107
|
T | C | 66 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0028others(63): Show | 88 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-111-2902A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584107 | ||||||
chr9:34584137
|
G | A | 13 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-111-2932C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584137 | ||||||
chr9:34584321
|
G | T | 80 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.-111-3116C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584321 | ||||||
chr9:34584465
|
C | T | 1 | a0001c0001t0003g0048 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-111-3260G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584465 | ||||||
chr9:34584629
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-111-3424T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584629 | ||||||
chr9:34584755
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-111-3550T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584755 | ||||||
chr9:34584780
|
A | ATGACCTC | 53 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0050others(50): Show | 74 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-111-3582_-111-357 others(11): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34584780 | ||||||
chr9:34585068
|
C | A | 1 | a0001c0001t0002g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-111-3863G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585068 | ||||||
chr9:34585387
|
G | A | 31 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0073others(28): Show | 36 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-112+4168C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585387 | ||||||
chr9:34585392
|
A | G | 1 | a0001c0002t0002g0237 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-112+4163T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585392 | ||||||
chr9:34585850
|
C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0052others(30): Show | 49 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-112+3705G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585850 | ||||||
chr9:34585854
|
CA | C | 13 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+3700delT | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585854 | ||||||
chr9:34585864
|
C | T | 22 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(19): Show | 32 | HG01255.hp1 HG01928.hp1 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.-112+3691G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585864 | ||||||
chr9:34585930
|
G | C | 18 | a0001c0001t0001g0028a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 22 | HG01175.hp2 HG02055.hp2 HG02572.hp1 others(19): Show |
intron_variant | MODIFIER | c.-112+3625C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585930 | ||||||
chr9:34585992
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-112+3563C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34585992 | ||||||
chr9:34586039
|
C | G | 1 | a0001c0001t0001g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112+3516G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586039 | ||||||
chr9:34586084
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-112+3471T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586084 | ||||||
chr9:34586136
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-112+3419C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586136 | ||||||
chr9:34586169
|
C | T | 17 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(14): Show | 27 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-112+3386G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586169 | ||||||
chr9:34586253
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-112+3302G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586253 | ||||||
chr9:34586279
|
C | A | 1 | a0001c0002t0002g0157 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-112+3276G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586279 | ||||||
chr9:34586346
|
A | T | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3209T>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586346 | ||||||
chr9:34586361
|
A | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3194T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586361 | ||||||
chr9:34586362
|
G | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3193C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586362 | ||||||
chr9:34586428
|
C | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3127G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586428 | ||||||
chr9:34586464
|
A | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+3091T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586464 | ||||||
chr9:34586469
|
C | T | 2 | a0001c0001t0001g0062a0001c0010t0001g0061 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-112+3086G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586469 | ||||||
chr9:34586491
|
T | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3064A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586491 | ||||||
chr9:34586492
|
T | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3063A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586492 | ||||||
chr9:34586493
|
C | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3062G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586493 | ||||||
chr9:34586495
|
C | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3060G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586495 | ||||||
chr9:34586497
|
C | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3058G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586497 | ||||||
chr9:34586498
|
C | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3057G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586498 | ||||||
chr9:34586499
|
C | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3056G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586499 | ||||||
chr9:34586500
|
C | T | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3055G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586500 | ||||||
chr9:34586502
|
C | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3053G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586502 | ||||||
chr9:34586503
|
C | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3052G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586503 | ||||||
chr9:34586504
|
C | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3051G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586504 | ||||||
chr9:34586507
|
C | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3048G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586507 | ||||||
chr9:34586508
|
C | G | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3047G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586508 | ||||||
chr9:34586509
|
T | A | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3046A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586509 | ||||||
chr9:34586512
|
G | T | 1 | a0001c0001t0008g0114 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-112+3043C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586512 | ||||||
chr9:34586542
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112+3013C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586542 | ||||||
chr9:34586605
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-112+2950T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586605 | ||||||
chr9:34586792
|
G | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(2): Show | 5 | NA18939.hp2 NA18946.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112+2763C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586792 | ||||||
chr9:34586816
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-112+2739A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586816 | ||||||
chr9:34586947
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02723.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-112+2608C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34586947 | ||||||
chr9:34587113
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-112+2442C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587113 | ||||||
chr9:34587243
|
C | A | 10 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+2312G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587243 | ||||||
chr9:34587312
|
T | A | 10 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+2243A>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587312 | ||||||
chr9:34587332
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-112+2223A>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587332 | ||||||
chr9:34587466
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-112+2089A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587466 | ||||||
chr9:34587487
|
C | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(52): Show | 70 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.-112+2068G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587487 | ||||||
chr9:34587689
|
C | T | 10 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0091others(7): Show | 10 | HG00741.hp2 HG01167.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112+1866G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587689 | ||||||
chr9:34587705
|
G | T | 13 | a0001c0001t0001g0027a0001c0001t0001g0073a0001c0001t0001g0078others(10): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-112+1850C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587705 | ||||||
chr9:34587808
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0234a0001c0001t0001g0235 | 6 | HG02083.hp1 HG02523.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112+1747C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34587808 | ||||||
chr9:34588008
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 252 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.-112+1547G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588008 | ||||||
chr9:34588013
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-112+1542C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588013 | ||||||
chr9:34588022
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-112+1533A>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588022 | ||||||
chr9:34588033
|
G | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0052others(30): Show | 49 | HG00544.hp1 HG00597.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-112+1522C>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588033 | ||||||
chr9:34588126
|
G | A | 6 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(3): Show | 8 | HG01074.hp1 HG01496.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-112+1429C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588126 | ||||||
chr9:34588240
|
C | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | HG01891.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-112+1315G>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588240 | ||||||
chr9:34588270
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-112+1285T>C | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588270 | ||||||
chr9:34588414
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112+1141G>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588414 | ||||||
chr9:34588509
|
G | A | 1 | a0001c0001t0001g0053 | 2 | NA19064.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-112+1046C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588509 | ||||||
chr9:34588509
|
G | T | 1 | a0001c0001t0005g0056 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-112+1046C>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588509 | ||||||
chr9:34588598
|
C | T | 1 | a0001c0001t0003g0074 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-112+957G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588598 | ||||||
chr9:34588607
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-112+948G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588607 | ||||||
chr9:34588621
|
C | CT | 4 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(1): Show | 4 | HG01891.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112+933dupA | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588621 | ||||||
chr9:34588696
|
GGGGAGGG others(6): Show |
G | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-112+846_-112+858d others(15): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588696 | ||||||
chr9:34588708
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112+847T>G | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588708 | ||||||
chr9:34588799
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-112+756G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34588799 | ||||||
chr9:34589054
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-112+501G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589054 | ||||||
chr9:34589057
|
GCA | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0062others(2): Show | 9 | HG01496.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112+496_-112+497d others(4): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589057 | ||||||
chr9:34589067
|
A | ACGCG | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG02258.hp2 HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-112+484_-112+487d others(6): Show |
CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589067 | ||||||
chr9:34589090
|
C | T | 1 | a0001c0001t0001g0267 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-112+465G>A | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589090 | ||||||
chr9:34589141
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0025others(14): Show | 27 | HG01928.hp1 HG01934.hp2 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.-112+414C>T | CNTFR | ENSG00000122756.15 | transcript | ENST00000378980.8 | protein_coding | 1/9 | chr9 | 34589141 |