Variant report
Variant | rs853037 |
---|---|
Chromosome Location | chr7:80603162-80603163 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:80601112..80603170-chr7:80604484..80606364,2 | MCF-7 | breast: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-SEMA3C-1 | chr7:80601832-80604040 | NONHSAT121756 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10242487 | 1.00[ASN][1000 genomes] |
rs10264043 | 1.00[ASN][1000 genomes] |
rs11977933 | 1.00[CHB][hapmap] |
rs12666421 | 1.00[CHB][hapmap] |
rs12671203 | 1.00[CHB][hapmap] |
rs12673546 | 1.00[CHB][hapmap] |
rs4259358 | 1.00[ASN][1000 genomes] |
rs471783 | 1.00[CHB][hapmap] |
rs4731944 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs492377 | 1.00[CHB][hapmap] |
rs500454 | 1.00[CHB][hapmap] |
rs512906 | 1.00[CHB][hapmap] |
rs517609 | 1.00[CHB][hapmap] |
rs551994 | 1.00[CHB][hapmap] |
rs767185 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs853034 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs853059 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs853060 | 1.00[ASN][1000 genomes] |
rs972504 | 1.00[ASN][1000 genomes] |
rs996720 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv888524 | chr7:80107798-80723062 | Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
2 | nsv1034690 | chr7:80520004-80987682 | Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
3 | nsv888549 | chr7:80553950-80652059 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv888550 | chr7:80584388-80644661 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv5812 | chr7:80601278-80645927 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:80597400-80604200 | Weak transcription | Aorta | Aorta |