Variant report
Variant | rs10877837 |
---|---|
Chromosome Location | chr12:40352614-40352615 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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rs_ID | r2[population] |
---|---|
rs10506145 | 1.00[JPT][hapmap] |
rs1086490 | 0.83[CEU][hapmap];1.00[JPT][hapmap] |
rs10877823 | 0.89[YRI][hapmap];0.89[AFR][1000 genomes] |
rs10877832 | 0.89[YRI][hapmap] |
rs11174315 | 0.87[YRI][hapmap] |
rs11174338 | 0.89[YRI][hapmap] |
rs11174370 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes] |
rs11174427 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11174532 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11174533 | 0.93[EUR][1000 genomes] |
rs11174536 | 0.80[EUR][1000 genomes] |
rs11514248 | 1.00[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11559994 | 0.89[YRI][hapmap];0.87[AFR][1000 genomes] |
rs11564133 | 1.00[JPT][hapmap] |
rs11564139 | 1.00[JPT][hapmap] |
rs11564160 | 1.00[JPT][hapmap] |
rs11564221 | 1.00[CEU][hapmap];0.98[EUR][1000 genomes] |
rs11564223 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs11564282 | 0.83[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes] |
rs11564285 | 0.89[YRI][hapmap] |
rs12230558 | 0.89[YRI][hapmap] |
rs12312535 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs12371119 | 1.00[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12810368 | 1.00[JPT][hapmap] |
rs12827948 | 1.00[JPT][hapmap] |
rs1482282 | 1.00[JPT][hapmap] |
rs17442304 | 1.00[JPT][hapmap] |
rs17442469 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs17442756 | 1.00[JPT][hapmap] |
rs17483628 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs17559478 | 1.00[JPT][hapmap] |
rs2046929 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs2404346 | 0.82[ASN][1000 genomes] |
rs2404574 | 1.00[JPT][hapmap] |
rs28370600 | 0.89[YRI][hapmap] |
rs28370607 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28370611 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28370644 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs28370654 | 0.82[ASN][1000 genomes] |
rs28370656 | 1.00[JPT][hapmap] |
rs28370659 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs28370681 | 0.82[ASN][1000 genomes] |
rs28370692 | 1.00[YRI][hapmap] |
rs28370728 | 0.89[YRI][hapmap] |
rs28740188 | 0.82[ASN][1000 genomes] |
rs28740190 | 1.00[YRI][hapmap] |
rs4399379 | 1.00[JPT][hapmap] |
rs55707305 | 0.82[ASN][1000 genomes] |
rs7297783 | 0.89[YRI][hapmap] |
rs7306718 | 1.00[JPT][hapmap] |
rs7316296 | 0.89[YRI][hapmap] |
rs73280629 | 0.86[EUR][1000 genomes] |
rs7484475 | 1.00[JPT][hapmap] |
rs7960023 | 0.87[AFR][1000 genomes] |
rs7969495 | 1.00[JPT][hapmap];0.82[ASN][1000 genomes] |
rs7974972 | 1.00[JPT][hapmap] |
rs992851 | 0.83[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1046428 | chr12:40226283-40439843 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
2 | nsv541481 | chr12:40226283-40439843 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1052202 | chr12:40322607-40406760 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription | Chromatin interactive regionmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:40338000-40366000 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
2 | chr12:40347800-40369800 | Weak transcription | Pancreas | Pancrea |
3 | chr12:40348200-40361400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr12:40352400-40354400 | Enhancers | Cortex derived primary cultured neurospheres | brain |