Variant report
Variant | rs11903055 |
---|---|
Chromosome Location | chr2:151198274-151198275 |
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 | chr2:151196792..151198427-chr2:151214963..151217254,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10497055 | 0.99[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11887785 | 0.80[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11903519 | 1.00[ASN][1000 genomes] |
rs16828091 | 1.00[ASN][1000 genomes] |
rs16828095 | 0.99[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs16828099 | 1.00[ASN][1000 genomes] |
rs16828101 | 1.00[ASN][1000 genomes] |
rs16828160 | 1.00[ASN][1000 genomes] |
rs17350215 | 0.90[EUR][1000 genomes] |
rs17350243 | 0.90[EUR][1000 genomes] |
rs17434648 | 0.93[EUR][1000 genomes] |
rs17434723 | 1.00[CEU][hapmap];0.90[EUR][1000 genomes] |
rs17434736 | 1.00[CEU][hapmap];0.90[EUR][1000 genomes] |
rs2119752 | 1.00[ASN][1000 genomes] |
rs66695478 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6717130 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72859536 | 1.00[EUR][1000 genomes] |
rs72859540 | 1.00[EUR][1000 genomes] |
rs72859568 | 1.00[EUR][1000 genomes] |
rs72859573 | 1.00[EUR][1000 genomes] |
rs72859575 | 1.00[EUR][1000 genomes] |
rs72859588 | 0.93[EUR][1000 genomes] |
rs72859591 | 0.93[EUR][1000 genomes] |
rs72859592 | 0.93[EUR][1000 genomes] |
rs72859596 | 0.93[EUR][1000 genomes] |
rs72859601 | 0.90[EUR][1000 genomes] |
rs72861403 | 0.90[EUR][1000 genomes] |
rs72861429 | 0.90[EUR][1000 genomes] |
rs72861435 | 0.90[EUR][1000 genomes] |
rs72861444 | 0.90[EUR][1000 genomes] |
rs72861451 | 0.87[EUR][1000 genomes] |
rs72861498 | 0.90[EUR][1000 genomes] |
rs72861502 | 0.90[EUR][1000 genomes] |
rs72864110 | 0.84[EUR][1000 genomes] |
rs72864111 | 0.84[EUR][1000 genomes] |
rs72864114 | 0.84[EUR][1000 genomes] |
rs72989965 | 0.99[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs72989969 | 1.00[ASN][1000 genomes] |
rs72989981 | 0.98[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs72989983 | 0.99[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs72993823 | 1.00[ASN][1000 genomes] |
rs7586993 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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 | nsv995119 | chr2:150556150-151294696 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv1001838 | chr2:150819672-151745876 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
3 | nsv535980 | chr2:150819672-151745876 | Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
4 | nsv532473 | chr2:151164210-151701860 | Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:151195600-151199600 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
2 | chr2:151198000-151198800 | Enhancers | Rectal Mucosa Donor 31 | rectum |
3 | chr2:151198200-151198600 | Enhancers | Brain Germinal Matrix | brain |