Variant report
Variant | rs11761491 |
---|---|
Chromosome Location | chr7:112306880-112306881 |
allele | A/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 | chr7:112306398..112307011-chr7:112509008..112509651,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10228483 | 0.83[AMR][1000 genomes] |
rs10232659 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10233896 | 0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10238492 | 0.82[CHB][hapmap] |
rs10249203 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10250630 | 0.81[AMR][1000 genomes] |
rs10261844 | 0.87[AMR][1000 genomes] |
rs10278994 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10280916 | 0.87[AMR][1000 genomes] |
rs11538991 | 0.81[AMR][1000 genomes] |
rs11763053 | 0.83[ASN][1000 genomes] |
rs11763216 | 0.86[ASN][1000 genomes] |
rs11769472 | 0.85[CHB][hapmap] |
rs11770706 | 1.00[CHB][hapmap] |
rs17581732 | 0.86[ASN][1000 genomes] |
rs1989834 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1989835 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2285541 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2396570 | 0.82[CHB][hapmap] |
rs3734956 | 0.83[AMR][1000 genomes] |
rs3957315 | 0.82[CHB][hapmap] |
rs4478510 | 1.00[CHB][hapmap] |
rs4582492 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56376790 | 0.87[AMR][1000 genomes] |
rs62475002 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62475004 | 0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs726593 | 0.85[CHB][hapmap] |
rs73436435 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs756867 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs756868 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs756869 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7796920 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7804823 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531436 | chr7:111856171-112585407 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 105 gene(s) | inside rSNPs | diseases |
2 | nsv889055 | chr7:112174089-112353440 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:112303000-112308000 | Weak transcription | Pancreas | Pancrea |