Variant report
Variant | rs1386356 |
---|---|
Chromosome Location | chr2:141032088-141032089 |
allele | A/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 | chr2:141030971..141033718-chr2:141035593..141037981,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10180435 | 0.96[CEU][hapmap] |
rs10195473 | 0.94[CHB][hapmap] |
rs10469558 | 1.00[CHB][hapmap] |
rs10469593 | 0.96[CEU][hapmap] |
rs10496839 | 0.93[CHB][hapmap] |
rs10496840 | 1.00[CHB][hapmap] |
rs10928746 | 0.83[ASN][1000 genomes] |
rs11895946 | 0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs12104972 | 0.96[CEU][hapmap] |
rs12464830 | 0.81[CHB][hapmap] |
rs12476338 | 0.83[ASN][1000 genomes] |
rs12477489 | 1.00[CHB][hapmap];0.83[ASN][1000 genomes] |
rs12479163 | 1.00[CHB][hapmap];0.83[ASN][1000 genomes] |
rs12612910 | 0.94[CHB][hapmap] |
rs13010738 | 0.94[CHB][hapmap] |
rs13021003 | 0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap] |
rs13413773 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs13424233 | 0.87[CHB][hapmap] |
rs1388809 | 0.94[CHB][hapmap] |
rs1486963 | 0.93[CHB][hapmap] |
rs1492393 | 1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap] |
rs1518441 | 1.00[CHB][hapmap] |
rs1532001 | 1.00[CHB][hapmap] |
rs2029628 | 0.81[CHB][hapmap] |
rs2171322 | 1.00[CHB][hapmap] |
rs2839772 | 0.91[CEU][hapmap];0.88[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs598786 | 0.93[CHB][hapmap] |
rs607494 | 1.00[CHB][hapmap] |
rs654051 | 0.93[CHB][hapmap] |
rs6717281 | 0.94[CHB][hapmap] |
rs6755822 | 0.94[CHB][hapmap] |
rs7340225 | 0.94[CHB][hapmap] |
rs7424028 | 0.87[CEU][hapmap] |
rs7567150 | 0.94[CHB][hapmap] |
rs7579083 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7581796 | 0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs982233 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834392 | chr2:140920900-141086613 | Flanking Active TSS Weak transcription Enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
2 | nsv431757 | chr2:140931289-141098020 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
3 | esv2754266 | chr2:141023643-141270786 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |