Variant report
Variant | rs16847368 |
---|---|
Chromosome Location | chr2:142611882-142611883 |
allele | C/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 | chr2:142601107..142603350-chr2:142610818..142614066,3 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10164495 | 0.90[CHB][hapmap] |
rs10496895 | 0.90[CHB][hapmap] |
rs10496901 | 0.90[CHB][hapmap] |
rs10496902 | 1.00[JPT][hapmap];0.81[YRI][hapmap] |
rs10928122 | 0.90[CHB][hapmap] |
rs1437339 | 0.90[CHB][hapmap] |
rs1437340 | 0.90[CHB][hapmap] |
rs16847095 | 0.90[CHB][hapmap] |
rs16847133 | 0.90[CHB][hapmap] |
rs16847142 | 0.90[CHB][hapmap] |
rs16847151 | 0.90[CHB][hapmap] |
rs16847202 | 0.90[CHB][hapmap] |
rs16847228 | 0.90[CHB][hapmap] |
rs16847265 | 0.90[CHB][hapmap];1.00[JPT][hapmap] |
rs16847310 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs16847314 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs16847347 | 0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap] |
rs16847376 | 0.91[CHB][hapmap];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs16847412 | 0.86[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap] |
rs1816608 | 0.90[CHB][hapmap] |
rs1946779 | 0.90[CHB][hapmap] |
rs61632456 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6748180 | 0.90[CHB][hapmap] |
rs7563727 | 0.90[CHB][hapmap] |
rs7584919 | 0.90[CHB][hapmap] |
rs7604400 | 0.90[CHB][hapmap] |
rs906640 | 0.81[CHB][hapmap] |
rs906641 | 0.86[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv530398 | chr2:142474842-142843839 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv875249 | chr2:142527100-142614345 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
3 | nsv875250 | chr2:142540240-142614345 | Enhancers Weak transcription | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
4 | nsv1009893 | chr2:142585905-142662116 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
5 | nsv459674 | chr2:142592560-142636907 | Weak transcription Enhancers Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
6 | nsv583237 | chr2:142592560-142636907 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:142609000-142613800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |