Variant report
Variant | rs12758057 |
---|---|
Chromosome Location | chr1:221832375-221832376 |
allele | A/G |
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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:221830865..221833221-chr1:221836408..221838119,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10449304 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11118800 | 0.89[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs11803842 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11807554 | 0.82[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs12118810 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12132407 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12134883 | 0.82[CHB][hapmap] |
rs12136282 | 0.86[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs12136283 | 0.86[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs12136513 | 0.84[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs12142693 | 0.92[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12728570 | 0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2095730 | 0.86[CHB][hapmap] |
rs2176690 | 0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs2378461 | 0.84[AFR][1000 genomes] |
rs6672743 | 0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs6685165 | 0.89[ASN][1000 genomes] |
rs66864883 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs67079790 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs68170611 | 0.86[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7532154 | 0.98[ASN][1000 genomes] |
rs7540426 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[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 | nsv997685 | chr1:220993527-221863416 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
2 | nsv535299 | chr1:220993527-221863416 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 28 gene(s) | inside rSNPs | diseases |
3 | nsv873200 | chr1:221644180-221843191 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:221832200-221832600 | Enhancers | GM12878-XiMat | blood |