Variant report
Variant | rs17400931 |
---|---|
Chromosome Location | chr2:178663294-178663295 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10497482 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12994400 | 0.80[ASN][1000 genomes] |
rs12994494 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13002444 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13004037 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs13004202 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13010041 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs13012088 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13018609 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs13021998 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs13026166 | 0.86[ASN][1000 genomes] |
rs13027484 | 0.86[ASN][1000 genomes] |
rs13033904 | 1.00[ASN][1000 genomes] |
rs1438064 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs16865819 | 0.83[EUR][1000 genomes] |
rs16865825 | 0.94[CEU][hapmap];0.81[EUR][1000 genomes] |
rs17329811 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs2083156 | 0.87[EUR][1000 genomes] |
rs2360221 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs34171827 | 1.00[ASN][1000 genomes] |
rs34356580 | 1.00[ASN][1000 genomes] |
rs34365395 | 0.87[EUR][1000 genomes] |
rs34956941 | 0.86[ASN][1000 genomes] |
rs35391362 | 1.00[ASN][1000 genomes] |
rs35586165 | 1.00[ASN][1000 genomes] |
rs35600620 | 0.87[ASN][1000 genomes] |
rs35873373 | 0.87[EUR][1000 genomes] |
rs3770054 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs4243392 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs4893988 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs4893989 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs56748987 | 0.87[EUR][1000 genomes] |
rs6433695 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6756606 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs71423505 | 1.00[ASN][1000 genomes] |
rs71423507 | 1.00[ASN][1000 genomes] |
rs71423508 | 1.00[ASN][1000 genomes] |
rs71423509 | 0.87[EUR][1000 genomes] |
rs71423514 | 0.86[ASN][1000 genomes] |
rs753346 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs7559765 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7588187 | 0.86[ASN][1000 genomes] |
rs7588301 | 1.00[CHB][hapmap];0.86[ASN][1000 genomes] |
rs7592278 | 1.00[ASN][1000 genomes] |
rs7592459 | 0.87[EUR][1000 genomes] |
rs7592731 | 0.81[EUR][1000 genomes] |
rs7595421 | 0.87[EUR][1000 genomes] |
rs7596644 | 0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7605744 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7609487 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs934803 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs934804 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999086 | chr2:178262348-178773585 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
2 | nsv536055 | chr2:178262348-178773585 | Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
3 | nsv583690 | chr2:178638381-178712283 | Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:178661600-178663400 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
2 | chr2:178662200-178664000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
3 | chr2:178663000-178664200 | Weak transcription | Psoas Muscle | Psoas |
4 | chr2:178663200-178664200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
5 | chr2:178663200-178664400 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
6 | chr2:178663200-178670000 | Weak transcription | Adipose Nuclei | Adipose |