Variant report
Variant | rs35710353 |
---|---|
Chromosome Location | chr5:108013544-108013545 |
allele | G/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 | chr5:108013253..108015897-chr5:108063039..108065514,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000272523 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10040128 | 0.81[EUR][1000 genomes] |
rs10063928 | 0.91[EUR][1000 genomes] |
rs12719098 | 0.82[EUR][1000 genomes] |
rs13169679 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13169987 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1355079 | 0.81[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2940517 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2940518 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs34251389 | 0.81[EUR][1000 genomes] |
rs34825344 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7707525 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs869287 | 0.86[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs9326743 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882689 | chr5:107595383-108299744 | Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 61 gene(s) | inside rSNPs | diseases |
2 | nsv1024076 | chr5:107991426-108028223 | Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1034158 | chr5:107995509-108018395 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | nsv523619 | chr5:107999505-108016782 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:108007000-108034800 | Weak transcription | Right Atrium | heart |