Variant report
Variant | rs4951727 |
---|---|
Chromosome Location | chr1:211342290-211342291 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:4)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:4 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | SETDB1 | chr1:211342212-211343078 | U2OS | brain: | n/a | n/a |
2 | CBX3 | chr1:211342178-211342503 | K562 | blood: | n/a | n/a |
3 | KAP1 | chr1:211342203-211342510 | HEK293 | kidney: | n/a | n/a |
4 | KAP1 | chr1:211342222-211343212 | K562 | blood: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000234004 | TF binding region |
rs_ID | r2[population] |
---|---|
rs12568832 | 0.81[ASN][1000 genomes] |
rs12749443 | 0.81[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs12758791 | 0.86[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs17017239 | 0.92[ASN][1000 genomes] |
rs2185069 | 0.92[ASN][1000 genomes] |
rs35286074 | 1.00[AFR][1000 genomes] |
rs35477371 | 1.00[AFR][1000 genomes] |
rs35505648 | 0.91[ASN][1000 genomes] |
rs35835736 | 0.81[ASN][1000 genomes] |
rs3811394 | 0.84[ASN][1000 genomes] |
rs4951506 | 1.00[AFR][1000 genomes] |
rs4951720 | 0.90[ASN][1000 genomes] |
rs4951725 | 0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs55824853 | 0.80[ASN][1000 genomes] |
rs56317037 | 0.80[ASN][1000 genomes] |
rs56367975 | 0.80[ASN][1000 genomes] |
rs71638201 | 1.00[AFR][1000 genomes] |
rs867847 | 0.92[ASN][1000 genomes] |
rs867848 | 0.92[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv945276 | chr1:211341161-211348032 | Enhancers ZNF genes & repeats Weak transcription Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:211342000-211342600 | Active TSS | Primary T cells from cord blood | blood |