Variant report
Variant | rs7128484 |
---|---|
Chromosome Location | chr11:16692990-16692991 |
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 | chr11:16691570..16693601-chr11:16731632..16734150,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10734249 | 0.92[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.89[EUR][1000 genomes] |
rs10741708 | 0.92[CEU][hapmap];0.87[EUR][1000 genomes] |
rs12786367 | 0.85[CEU][hapmap] |
rs12794768 | 0.94[EUR][1000 genomes] |
rs12799800 | 0.98[EUR][1000 genomes] |
rs12799969 | 0.97[EUR][1000 genomes] |
rs12804277 | 0.94[EUR][1000 genomes] |
rs1501451 | 0.95[EUR][1000 genomes] |
rs1846936 | 1.00[CEU][hapmap];0.93[EUR][1000 genomes] |
rs1967192 | 0.98[EUR][1000 genomes] |
rs1995343 | 0.93[EUR][1000 genomes] |
rs2221243 | 0.85[EUR][1000 genomes] |
rs34097789 | 0.94[EUR][1000 genomes] |
rs34812104 | 0.94[EUR][1000 genomes] |
rs3802963 | 1.00[CEU][hapmap];0.93[EUR][1000 genomes] |
rs3921675 | 0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs4396254 | 0.85[CEU][hapmap];0.94[CHB][hapmap];0.81[JPT][hapmap] |
rs4756860 | 0.89[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4756862 | 0.95[EUR][1000 genomes] |
rs4757428 | 0.83[EUR][1000 genomes] |
rs4757431 | 0.93[GIH][hapmap];0.81[JPT][hapmap];0.86[TSI][hapmap] |
rs4757432 | 0.81[EUR][1000 genomes] |
rs6486310 | 0.89[EUR][1000 genomes] |
rs6486312 | 0.95[EUR][1000 genomes] |
rs66670205 | 0.87[EUR][1000 genomes] |
rs7110136 | 0.92[CEU][hapmap];0.86[GIH][hapmap];0.87[TSI][hapmap];0.87[EUR][1000 genomes] |
rs7117140 | 0.95[EUR][1000 genomes] |
rs7125008 | 0.82[EUR][1000 genomes] |
rs7125262 | 1.00[CEU][hapmap];0.86[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7939889 | 0.89[EUR][1000 genomes] |
rs7944906 | 0.93[EUR][1000 genomes] |
rs7945007 | 0.81[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv553566 | chr11:16329009-16799044 | Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
2 | esv3396970 | chr11:16658425-16715569 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:16692200-16700200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |