Variant report
Variant | rs450401 |
---|---|
Chromosome Location | chr6:164471335-164471336 |
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 | chr6:164445952..164448558-chr6:164471088..164472960,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs11757045 | 1.00[CHB][hapmap] |
rs183268 | 1.00[AMR][1000 genomes] |
rs205997 | 1.00[AMR][1000 genomes] |
rs206000 | 1.00[AMR][1000 genomes] |
rs206689 | 1.00[AMR][1000 genomes] |
rs206690 | 1.00[AMR][1000 genomes] |
rs206698 | 1.00[AMR][1000 genomes] |
rs206724 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs206725 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs206727 | 1.00[YRI][hapmap];1.00[AMR][1000 genomes] |
rs369452 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs373183 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs374320 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs383614 | 1.00[AMR][1000 genomes] |
rs383720 | 1.00[AMR][1000 genomes] |
rs384008 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs394999 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs395240 | 1.00[AMR][1000 genomes] |
rs409958 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs410781 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs413058 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs444176 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs445024 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs446252 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs449084 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs451353 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs454476 | 1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs655061 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1018860 | chr6:163939347-164532579 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
2 | nsv538526 | chr6:163939347-164532579 | Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
3 | nsv1026707 | chr6:164188210-164749206 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | nsv538527 | chr6:164188210-164749206 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | nsv1019703 | chr6:164424683-164488780 | Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1029952 | chr6:164463355-165268911 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:164470400-164471600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |