Variant report
Variant | rs61502427 |
---|---|
Chromosome Location | chr1:47561826-47561827 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11488318 | 1.00[EUR][1000 genomes] |
rs12085485 | 1.00[EUR][1000 genomes] |
rs12092838 | 1.00[EUR][1000 genomes] |
rs12096366 | 1.00[EUR][1000 genomes] |
rs56311064 | 1.00[EUR][1000 genomes] |
rs58921777 | 1.00[EUR][1000 genomes] |
rs59550357 | 1.00[EUR][1000 genomes] |
rs60589829 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs72894542 | 1.00[EUR][1000 genomes] |
rs72894554 | 1.00[EUR][1000 genomes] |
rs72894561 | 1.00[EUR][1000 genomes] |
rs72894575 | 1.00[EUR][1000 genomes] |
rs74073558 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74073585 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74073742 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74073791 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74073793 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs74073879 | 1.00[EUR][1000 genomes] |
rs74073880 | 1.00[EUR][1000 genomes] |
rs74076309 | 1.00[EUR][1000 genomes] |
rs74076312 | 1.00[EUR][1000 genomes] |
rs74076314 | 1.00[EUR][1000 genomes] |
rs74076315 | 1.00[EUR][1000 genomes] |
rs74077366 | 1.00[EUR][1000 genomes] |
rs9333021 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2763300 | chr1:47358532-47628774 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv916813 | chr1:47435635-47666179 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
3 | nsv870705 | chr1:47533705-47620126 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv871010 | chr1:47533705-47637999 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv870899 | chr1:47548974-47637999 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:47557800-47573800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |