Variant report
Variant | rs6924093 |
---|---|
Chromosome Location | chr6:25864170-25864171 |
allele | A/C |
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 | chr6:25858832..25860759-chr6:25863922..25867264,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs199757 | 1.00[MEX][hapmap] |
rs28433902 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4379284 | 1.00[EUR][1000 genomes] |
rs4484510 | 1.00[EUR][1000 genomes] |
rs6914607 | 1.00[TSI][hapmap] |
rs6927402 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6928040 | 1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs6928384 | 1.00[MEX][hapmap] |
rs6933573 | 1.00[LWK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs6933725 | 1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs73383224 | 1.00[EUR][1000 genomes] |
rs73383248 | 1.00[EUR][1000 genomes] |
rs73383256 | 1.00[EUR][1000 genomes] |
rs73383283 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73383287 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73385003 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73385005 | 1.00[EUR][1000 genomes] |
rs73385008 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73385013 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73385016 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73385046 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73385068 | 1.00[EUR][1000 genomes] |
rs73385070 | 1.00[EUR][1000 genomes] |
rs73385071 | 1.00[EUR][1000 genomes] |
rs7741430 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7750960 | 0.82[YRI][hapmap] |
rs7765800 | 1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7766892 | 1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs7776337 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs807213 | 1.00[MEX][hapmap] |
rs9358868 | 1.00[MEX][hapmap];1.00[TSI][hapmap] |
rs9393666 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1029920 | chr6:25638507-26585842 | Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1215 gene(s) | inside rSNPs | diseases |
2 | nsv538162 | chr6:25638507-26585842 | Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1215 gene(s) | inside rSNPs | diseases |
3 | nsv427747 | chr6:25641380-25908218 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
4 | nsv1030351 | chr6:25813178-26352046 | Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1189 gene(s) | inside rSNPs | diseases |
5 | nsv1023453 | chr6:25853830-26528250 | Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 1201 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:25863200-25864600 | Enhancers | HepG2 | liver |
2 | chr6:25863800-25864600 | Flanking Active TSS | Liver | Liver |