Variant report
Variant | rs6984456 |
---|---|
Chromosome Location | chr8:67267364-67267365 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-RRS1-3 | chr8:67266900-67267756 | ucscGeneNc_uc003xvz_1 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10095385 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17404672 | 0.87[ASN][1000 genomes] |
rs1978566 | 0.91[CEU][hapmap] |
rs2114487 | 0.87[ASN][1000 genomes] |
rs2162420 | 0.87[ASN][1000 genomes] |
rs56332328 | 0.87[ASN][1000 genomes] |
rs56747323 | 0.87[ASN][1000 genomes] |
rs57935379 | 0.87[ASN][1000 genomes] |
rs7015255 | 1.00[JPT][hapmap] |
rs73691528 | 0.87[ASN][1000 genomes] |
rs7834793 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7846153 | 0.87[ASN][1000 genomes] |
rs9693831 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3446467 | chr8:66749863-67667068 | Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 73 gene(s) | inside rSNPs | diseases |
2 | esv3414665 | chr8:66936816-67381935 | Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs6984456 | ADHFE1 | cis | Thyroid | GTEx |
rs6984456 | C8orf46 | cis | Adipose Subcutaneous | GTEx |
rs6984456 | ADHFE1 | cis | Nerve Tibial | GTEx |
rs6984456 | C8orf46 | cis | Esophagus Muscularis | GTEx |
rs6984456 | C8orf46 | cis | Thyroid | GTEx |
rs6984456 | ADHFE1 | cis | Artery Tibial | GTEx |
rs6984456 | ADHFE1 | cis | Skin Sun Exposed Lower leg | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:67265400-67268800 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |