Variant report
Variant | rs12699241 |
---|---|
Chromosome Location | chr7:11612083-11612084 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10242744 | 0.82[JPT][hapmap] |
rs10250564 | 0.82[JPT][hapmap] |
rs10486153 | 0.89[CHB][hapmap];0.91[CHD][hapmap] |
rs10486154 | 0.84[CEU][hapmap];0.84[GIH][hapmap];0.82[JPT][hapmap];0.94[MEX][hapmap];0.82[MKK][hapmap];0.88[TSI][hapmap] |
rs12699211 | 0.82[JPT][hapmap] |
rs12699236 | 0.89[ASN][1000 genomes] |
rs12699238 | 0.84[CEU][hapmap];0.80[CHD][hapmap];0.93[GIH][hapmap];0.89[MEX][hapmap];0.87[AMR][1000 genomes] |
rs12699240 | 0.89[CEU][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12699242 | 0.87[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12699243 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes] |
rs12699244 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs12699245 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs12699246 | 0.95[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap] |
rs12699247 | 0.95[CHB][hapmap];0.82[JPT][hapmap] |
rs13229007 | 0.84[CHB][hapmap];0.85[ASN][1000 genomes] |
rs13229378 | 0.81[CHB][hapmap];0.85[ASN][1000 genomes] |
rs13229567 | 0.85[ASN][1000 genomes] |
rs13240026 | 0.88[MEX][hapmap] |
rs13246013 | 0.93[ASN][1000 genomes] |
rs17164805 | 0.80[CHD][hapmap] |
rs17164823 | 0.89[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes] |
rs68035468 | 0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6980325 | 0.84[CHB][hapmap];0.84[ASN][1000 genomes] |
rs764195 | 0.88[CHD][hapmap] |
rs7777369 | 0.84[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.89[MEX][hapmap];0.82[TSI][hapmap];0.89[ASN][1000 genomes] |
rs7785852 | 0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1028326 | chr7:11221209-11754436 | Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv538733 | chr7:11221209-11754436 | Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv1023665 | chr7:11457493-11773517 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv887606 | chr7:11473561-11771288 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv606199 | chr7:11506143-12486659 | Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:11577400-11615200 | Weak transcription | Placenta | Placenta |
2 | chr7:11609200-11613400 | Enhancers | Liver | Liver |
3 | chr7:11610600-11613400 | Weak transcription | A549 | lung |