Variant report
Variant | rs6847622 |
---|---|
Chromosome Location | chr4:48465334-48465335 |
allele | A/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 | chr4:48461047..48463475-chr4:48463503..48465946,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10517218 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10805169 | 0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs13101954 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs13102023 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13105648 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13110633 | 0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs13114836 | 0.81[EUR][1000 genomes] |
rs13139251 | 0.93[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13139533 | 0.89[EUR][1000 genomes] |
rs13142082 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs13145713 | 0.82[EUR][1000 genomes] |
rs1565217 | 0.80[EUR][1000 genomes] |
rs17472127 | 0.90[CHB][hapmap];0.82[EUR][1000 genomes] |
rs2029347 | 0.80[ASN][1000 genomes] |
rs2291476 | 0.80[ASN][1000 genomes] |
rs28840724 | 0.80[ASN][1000 genomes] |
rs34239305 | 0.80[ASN][1000 genomes] |
rs34380340 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34386102 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs34922671 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs35079648 | 0.93[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs35963236 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs3811759 | 0.82[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes] |
rs3943122 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes] |
rs409911 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs62311260 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6447639 | 0.94[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6819847 | 0.83[ASN][1000 genomes] |
rs6821909 | 0.81[EUR][1000 genomes] |
rs6824075 | 0.90[EUR][1000 genomes] |
rs6824125 | 0.83[CEU][hapmap];0.90[CHB][hapmap];0.90[EUR][1000 genomes] |
rs6844692 | 0.80[EUR][1000 genomes] |
rs6845250 | 0.90[EUR][1000 genomes] |
rs73246023 | 0.83[ASN][1000 genomes] |
rs745761 | 0.86[JPT][hapmap];0.80[EUR][1000 genomes] |
rs7670045 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7676578 | 0.89[EUR][1000 genomes] |
rs7698564 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv470034 | chr4:48427773-48605628 | Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 7 gene(s) | inside rSNPs | diseases |
2 | nsv594121 | chr4:48427773-48605628 | Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 7 gene(s) | inside rSNPs | diseases |
3 | nsv1005268 | chr4:48444307-48484389 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv537086 | chr4:48444307-48484389 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:48464400-48465400 | Enhancers | Brain Germinal Matrix | brain |
2 | chr4:48464400-48471600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |