Variant report
Variant | rs1948988 |
---|---|
Chromosome Location | chr12:75080657-75080658 |
allele | 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 | chr12:74931373..74934203-chr12:75080522..75082837,2 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000253719 | Chromatin interaction |
ENSG00000257386 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10506689 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10785138 | 0.92[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap] |
rs10879820 | 0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10879821 | 0.90[CEU][hapmap];0.93[CHB][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.97[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1112143 | 0.93[ASN][1000 genomes] |
rs11180159 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11180162 | 1.00[CEU][hapmap];0.93[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11180164 | 0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11180166 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12231259 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2063182 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv899297 | chr12:75045728-75169675 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv899298 | chr12:75045728-75173289 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv427915 | chr12:75047293-75172692 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |