Variant report
Variant | rs2299526 |
---|---|
Chromosome Location | chr7:126665324-126665325 |
allele | A/C/T |
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:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | 7:126085913-126088095..7:126662926-126671620 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000179603 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10268335 | 0.91[EUR][1000 genomes] |
rs10487464 | 0.91[EUR][1000 genomes] |
rs10487465 | 0.91[EUR][1000 genomes] |
rs10487466 | 0.91[EUR][1000 genomes] |
rs11563750 | 0.91[EUR][1000 genomes] |
rs11563755 | 0.91[EUR][1000 genomes] |
rs11563756 | 0.91[EUR][1000 genomes] |
rs11563757 | 0.91[EUR][1000 genomes] |
rs11563758 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs11563759 | 0.91[EUR][1000 genomes] |
rs11563760 | 0.89[EUR][1000 genomes] |
rs11563761 | 0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs11563782 | 0.83[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs12669516 | 0.91[EUR][1000 genomes] |
rs17644601 | 0.89[AMR][1000 genomes] |
rs17862270 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17862277 | 0.91[EUR][1000 genomes] |
rs17863187 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs17864094 | 0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17864106 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17874838 | 0.91[EUR][1000 genomes] |
rs2237781 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62468871 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62468872 | 0.91[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs6958658 | 0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758132 | chr7:126494789-126677843 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | esv2759562 | chr7:126494789-126677843 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv427805 | chr7:126494789-126677843 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv831121 | chr7:126593363-126774413 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 6 gene(s) | inside rSNPs | diseases |
No data |