Variant report
Variant | rs17047774 |
---|---|
Chromosome Location | chr3:68553116-68553117 |
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 | chr3:68548311..68550713-chr3:68552898..68555029,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10514723 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap] |
rs11713541 | 0.82[YRI][hapmap] |
rs11925200 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs17047708 | 0.94[JPT][hapmap] |
rs17047742 | 0.90[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes] |
rs17047807 | 1.00[MEX][hapmap] |
rs2036811 | 0.83[ASN][1000 genomes] |
rs2036812 | 0.85[ASN][1000 genomes] |
rs2202976 | 0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.85[YRI][hapmap];0.91[ASN][1000 genomes] |
rs4855488 | 0.92[YRI][hapmap] |
rs56064707 | 0.93[ASN][1000 genomes] |
rs56285685 | 0.83[ASN][1000 genomes] |
rs59001415 | 0.89[ASN][1000 genomes] |
rs6771965 | 0.89[JPT][hapmap];0.90[LWK][hapmap];0.80[MKK][hapmap];0.89[YRI][hapmap] |
rs6772010 | 0.87[LWK][hapmap];0.83[MKK][hapmap];0.89[YRI][hapmap] |
rs6804619 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6809703 | 0.81[YRI][hapmap];0.92[ASN][1000 genomes] |
rs72921003 | 0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs73837656 | 0.93[ASN][1000 genomes] |
rs907081 | 0.82[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1832396 | chr3:68478762-68641509 | Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv876929 | chr3:68508137-68565824 | ZNF genes & repeats Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:68552600-68554000 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |