Variant report
Variant | rs780558 |
---|---|
Chromosome Location | chr6:49796911-49796912 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:4)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:4 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:49795036..49797729-chr6:49810311..49812843,2 | K562 | blood: | |
2 | chr6:49796837..49798600-chr6:49802108..49804772,2 | K562 | blood: | |
3 | chr6:49795036..49798204-chr6:49810263..49813225,4 | K562 | blood: | |
4 | chr6:49789364..49791456-chr6:49796213..49798004,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1084052 | 0.88[ASW][hapmap];1.00[CEU][hapmap];0.86[JPT][hapmap];0.93[MEX][hapmap] |
rs12205447 | 0.82[JPT][hapmap] |
rs1417491 | 0.88[ASW][hapmap];1.00[CEU][hapmap];0.91[JPT][hapmap];0.93[MEX][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs2153575 | 0.93[EUR][1000 genomes] |
rs2396920 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs3799689 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6913978 | 0.86[JPT][hapmap] |
rs780553 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9473663 | 0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv933942 | chr6:49480550-50004231 | Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
2 | nsv933833 | chr6:49515134-49961765 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No data |