Variant report
Variant | rs10500562 |
---|---|
Chromosome Location | chr16:71627731-71627732 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:5)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:5 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr16:71599003..71601212-chr16:71626503..71628905,3 | MCF-7 | breast: | |
2 | chr16:71619005..71622158-chr16:71624497..71628582,3 | MCF-7 | breast: | |
3 | chr16:71610910..71613434-chr16:71625307..71628011,2 | MCF-7 | breast: | |
4 | chr16:71620059..71623986-chr16:71624555..71628126,4 | K562 | blood: | |
5 | chr16:71617743..71620944-chr16:71623510..71629650,6 | MCF-7 | breast: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000260886 | Chromatin interaction |
ENSG00000198650 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs12149264 | 0.90[CEU][hapmap];1.00[YRI][hapmap] |
rs12444890 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs12446333 | 0.91[CEU][hapmap] |
rs12447033 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs12447672 | 0.81[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs12919417 | 0.81[CEU][hapmap];0.81[AMR][1000 genomes] |
rs12922775 | 1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs12923781 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12924650 | 0.91[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes] |
rs12927006 | 0.91[CEU][hapmap] |
rs12927456 | 0.91[CEU][hapmap] |
rs12927768 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12931191 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs12935422 | 0.97[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs17282500 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17345863 | 0.89[CEU][hapmap] |
rs17347255 | 1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs17354693 | 0.91[CEU][hapmap];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs17355804 | 0.91[CEU][hapmap];1.00[YRI][hapmap] |
rs17356206 | 0.86[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes] |
rs17356316 | 0.91[CEU][hapmap] |
rs34181942 | 0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs34381861 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs34753286 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs35538253 | 0.97[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs71403859 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs7203606 | 1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs8051974 | 0.91[CEU][hapmap] |
rs8053720 | 0.81[CEU][hapmap] |
rs8063455 | 1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3347477 | chr16:71555148-71985177 | Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
2 | nsv1063338 | chr16:71612346-71752968 | Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:71627200-71628600 | Flanking Active TSS | HepG2 | liver |
2 | chr16:71627400-71630400 | Enhancers | Liver | Liver |