Variant report
Variant | rs7721136 |
---|---|
Chromosome Location | chr5:42000952-42000953 |
allele | C/T |
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 | chr5:41925201..41926819-chr5:41999709..42001806,2 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000151876 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10941559 | 0.82[EUR][1000 genomes] |
rs11739106 | 0.81[EUR][1000 genomes] |
rs11739257 | 0.81[EUR][1000 genomes] |
rs11740524 | 0.81[EUR][1000 genomes] |
rs11742249 | 0.80[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs11744623 | 0.82[EUR][1000 genomes] |
rs11746511 | 0.81[EUR][1000 genomes] |
rs11750607 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs13153837 | 0.81[EUR][1000 genomes] |
rs13156367 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs13164201 | 0.81[EUR][1000 genomes] |
rs13167578 | 0.89[EUR][1000 genomes] |
rs13170096 | 0.88[EUR][1000 genomes] |
rs13180405 | 0.88[EUR][1000 genomes] |
rs1508818 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16871972 | 0.81[EUR][1000 genomes] |
rs16900142 | 0.82[EUR][1000 genomes] |
rs1876653 | 0.82[EUR][1000 genomes] |
rs1876654 | 0.80[EUR][1000 genomes] |
rs35244816 | 0.88[EUR][1000 genomes] |
rs35613904 | 0.82[EUR][1000 genomes] |
rs35748945 | 0.89[EUR][1000 genomes] |
rs36009913 | 0.87[EUR][1000 genomes] |
rs4957430 | 0.81[EUR][1000 genomes] |
rs66820325 | 0.81[EUR][1000 genomes] |
rs67869805 | 0.81[EUR][1000 genomes] |
rs6865448 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6881206 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6881873 | 0.81[EUR][1000 genomes] |
rs7725264 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9687619 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830273 | chr5:41867296-42066070 | Flanking Active TSS Active TSS Genic enhancers Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 111 gene(s) | inside rSNPs | diseases |
2 | nsv933208 | chr5:41879946-42876624 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 112 gene(s) | inside rSNPs | diseases |
3 | nsv492147 | chr5:41902086-42896162 | Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 113 gene(s) | inside rSNPs | diseases |
4 | nsv880627 | chr5:41966551-42087954 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 5 gene(s) | inside rSNPs | diseases |