Variant report
Variant | rs16931360 |
---|---|
Chromosome Location | chr8:65580861-65580862 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:65579416..65581773-chr8:65583338..65585855,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10098783 | 0.82[CHB][hapmap];0.81[CHD][hapmap];0.80[JPT][hapmap] |
rs10283033 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs10957319 | 0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13271194 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs13276281 | 0.87[CEU][hapmap];0.82[CHB][hapmap];0.90[CHD][hapmap];0.88[EUR][1000 genomes] |
rs13278548 | 0.82[EUR][1000 genomes] |
rs1451869 | 0.87[CEU][hapmap];0.82[CHB][hapmap];0.90[CHD][hapmap];0.88[EUR][1000 genomes] |
rs16931350 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs16931358 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16931363 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2356986 | 0.82[CHB][hapmap];0.80[JPT][hapmap] |
rs2884074 | 0.81[CHB][hapmap] |
rs3779869 | 0.87[CEU][hapmap];0.82[CHB][hapmap];0.88[EUR][1000 genomes] |
rs3824188 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4236936 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs4258041 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs4269577 | 0.82[CHB][hapmap];0.81[CHD][hapmap] |
rs4392942 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs4397440 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap] |
rs4527914 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap] |
rs4549812 | 0.82[CHB][hapmap];0.81[CHD][hapmap];0.80[JPT][hapmap] |
rs4737682 | 0.82[CHB][hapmap];0.81[CHD][hapmap];0.80[JPT][hapmap] |
rs60471153 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6472151 | 0.82[CHB][hapmap];0.81[CHD][hapmap] |
rs6987861 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs7004523 | 1.00[ASW][hapmap] |
rs7821085 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs7822429 | 0.87[CEU][hapmap];0.82[CHB][hapmap];0.90[CHD][hapmap];0.88[EUR][1000 genomes] |
rs7829301 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |
rs7842113 | 0.91[CHB][hapmap];0.80[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534001 | chr8:64992196-65798776 | Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 17 gene(s) | inside rSNPs | diseases |
2 | esv1847262 | chr8:65509694-65595527 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv6231 | chr8:65538593-65583623 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | esv2761434 | chr8:65578467-66567678 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
5 | esv3444272 | chr8:65580428-65580938 | Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:65571400-65585400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |