Variant report
Variant | rs6972054 |
---|---|
Chromosome Location | chr7:84467186-84467187 |
allele | C/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 | chr7:84465310..84468926-chr7:84469765..84473361,5 | K562 | blood: | |
2 | chr7:84465946..84467768-chr7:84474017..84476802,2 | K562 | blood: | |
3 | chr7:84466265..84469196-chr7:84470899..84473576,3 | K562 | blood: | |
4 | chr7:84459040..84461064-chr7:84467075..84469112,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10224730 | 0.83[ASN][1000 genomes] |
rs10225306 | 0.82[ASN][1000 genomes] |
rs10227116 | 0.83[ASN][1000 genomes] |
rs10229754 | 0.83[ASN][1000 genomes] |
rs10240021 | 0.83[ASN][1000 genomes] |
rs10272662 | 0.82[ASN][1000 genomes] |
rs1030540 | 0.83[ASN][1000 genomes] |
rs10499882 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11984418 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs12538302 | 0.80[ASN][1000 genomes] |
rs12707682 | 0.82[ASN][1000 genomes] |
rs12707683 | 0.82[ASN][1000 genomes] |
rs13227983 | 0.82[ASN][1000 genomes] |
rs1583136 | 0.82[ASN][1000 genomes] |
rs1583137 | 0.82[ASN][1000 genomes] |
rs1594393 | 0.83[ASN][1000 genomes] |
rs1609876 | 0.81[ASN][1000 genomes] |
rs1897158 | 0.83[ASN][1000 genomes] |
rs34107456 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs35508218 | 0.82[ASN][1000 genomes] |
rs35715078 | 0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs35895941 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs35992683 | 0.82[ASN][1000 genomes] |
rs4301393 | 0.83[ASN][1000 genomes] |
rs62474471 | 0.83[ASN][1000 genomes] |
rs62474494 | 0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6946368 | 0.84[ASN][1000 genomes] |
rs7458400 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7803475 | 0.82[ASN][1000 genomes] |
rs9649677 | 0.83[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv529344 | chr7:83714286-84592857 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
2 | nsv949446 | chr7:84003501-84763823 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
3 | nsv831049 | chr7:84277599-84475710 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
4 | esv34238 | chr7:84279023-84591966 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv831050 | chr7:84355996-84527261 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:84466800-84467200 | Enhancers | K562 | blood |
2 | chr7:84466800-84467400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |