Variant report
Variant | rs2643365 |
---|---|
Chromosome Location | chr15:33871487-33871488 |
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 | chr15:33870139..33872552-chr17:56728731..56731471,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1030770 | 0.86[JPT][hapmap] |
rs1030771 | 0.87[JPT][hapmap] |
rs11630933 | 0.87[JPT][hapmap] |
rs11633042 | 0.93[ASN][1000 genomes] |
rs11634054 | 0.91[JPT][hapmap] |
rs12439812 | 0.86[JPT][hapmap] |
rs12899789 | 0.91[JPT][hapmap];0.84[ASN][1000 genomes] |
rs1369310 | 0.91[JPT][hapmap] |
rs1435117 | 0.99[ASN][1000 genomes] |
rs1435118 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs1435121 | 0.86[JPT][hapmap] |
rs1435122 | 0.91[JPT][hapmap] |
rs1435123 | 0.91[JPT][hapmap] |
rs1594955 | 0.91[JPT][hapmap];0.84[ASN][1000 genomes] |
rs1865499 | 0.91[JPT][hapmap] |
rs2060453 | 0.86[JPT][hapmap] |
rs2339307 | 0.91[JPT][hapmap] |
rs2339309 | 0.91[JPT][hapmap] |
rs2339310 | 0.91[JPT][hapmap] |
rs2437136 | 0.95[ASN][1000 genomes] |
rs3829476 | 0.91[JPT][hapmap] |
rs3829477 | 0.91[JPT][hapmap] |
rs3829478 | 0.91[JPT][hapmap] |
rs4503763 | 0.91[JPT][hapmap] |
rs4779621 | 0.82[ASN][1000 genomes] |
rs4780127 | 0.84[ASN][1000 genomes] |
rs589134 | 0.94[ASN][1000 genomes] |
rs603657 | 0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs604934 | 0.94[ASN][1000 genomes] |
rs605682 | 0.95[ASN][1000 genomes] |
rs606639 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes] |
rs619196 | 0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes] |
rs620150 | 0.96[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs620644 | 0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs622365 | 0.94[ASN][1000 genomes] |
rs666342 | 0.94[ASN][1000 genomes] |
rs674155 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs680388 | 0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs680792 | 0.94[ASN][1000 genomes] |
rs680851 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs682639 | 0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs683141 | 0.94[ASN][1000 genomes] |
rs683484 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs683553 | 0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs7164455 | 0.91[JPT][hapmap] |
rs7167970 | 0.97[ASN][1000 genomes] |
rs7169123 | 0.97[ASN][1000 genomes] |
rs7170881 | 0.91[JPT][hapmap] |
rs7172763 | 0.91[JPT][hapmap] |
rs721667 | 0.91[JPT][hapmap] |
rs8030946 | 0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs8033477 | 0.91[JPT][hapmap];0.82[ASN][1000 genomes] |
rs9635321 | 0.97[ASN][1000 genomes] |
rs968275 | 0.86[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs9806564 | 0.94[ASN][1000 genomes] |
rs9806613 | 0.80[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1043046 | chr15:33714908-34321330 | Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | esv34041 | chr15:33720726-33871487 | Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | esv34037 | chr15:33732616-34049083 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr15:33827400-33877200 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
2 | chr15:33846400-33872000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr15:33858000-33921200 | Weak transcription | Stomach Smooth Muscle | stomach |
4 | chr15:33858600-33895200 | Weak transcription | Fetal Muscle Leg | muscle |
5 | chr15:33859200-33923200 | Weak transcription | Fetal Muscle Trunk | muscle |
6 | chr15:33871400-33872200 | Weak transcription | Ovary | ovary |