Variant report
Variant | rs10259052 |
---|---|
Chromosome Location | chr7:122182665-122182666 |
allele | C/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:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:122182067..122184519-chr7:122256658..122258935,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10229609 | 1.00[YRI][hapmap] |
rs10235626 | 0.87[YRI][hapmap] |
rs10238269 | 0.87[YRI][hapmap] |
rs10253515 | 1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10258166 | 0.87[YRI][hapmap] |
rs10258309 | 0.87[YRI][hapmap] |
rs10258422 | 1.00[YRI][hapmap] |
rs10269952 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10271472 | 0.87[YRI][hapmap] |
rs10281006 | 1.00[YRI][hapmap] |
rs10441358 | 1.00[YRI][hapmap] |
rs11974367 | 1.00[YRI][hapmap] |
rs11974506 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17380636 | 0.87[YRI][hapmap] |
rs28393630 | 1.00[AMR][1000 genomes] |
rs28408353 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs28450014 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6947978 | 1.00[YRI][hapmap] |
rs6949079 | 1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6952265 | 1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs6954982 | 1.00[ASW][hapmap];0.91[MKK][hapmap];1.00[YRI][hapmap] |
rs6980172 | 0.87[YRI][hapmap] |
rs73218218 | 0.94[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1017029 | chr7:121958574-122338623 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | esv3418472 | chr7:122180941-122182964 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:122182600-122183200 | Enhancers | Fetal Lung | lung |