Variant report
Variant | rs2244072 |
---|---|
Chromosome Location | chr1:220459758-220459759 |
allele | C/T |
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 | chr1:220437133..220439238-chr1:220458442..220459950,2 | K562 | blood: | |
2 | chr1:220448590..220453578-chr1:220456317..220461314,5 | K562 | blood: | |
3 | chr1:220453040..220456116-chr1:220457163..220460611,3 | K562 | blood: | |
4 | chr1:220443856..220448650-chr1:220458115..220462715,5 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000118873 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10779403 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs11118517 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs11118519 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12409579 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs12411005 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1473073 | 0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs17007362 | 0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs4846621 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs61830458 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs61832260 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs61832262 | 0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6541128 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6541130 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs7529864 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7554794 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9793772 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001681 | chr1:220425057-220548325 | Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv535298 | chr1:220425057-220548325 | Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:220457600-220463600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |