Variant report
Variant | rs12209100 |
---|---|
Chromosome Location | chr6:132855963-132855964 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:14)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:14 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | FOXA1 | chr6:132855658-132856078 | HepG2 | liver: | n/a | n/a |
2 | FOXA1 | chr6:132855645-132856084 | HepG2 | liver: | n/a | n/a |
3 | FOXA1 | chr6:132855675-132856056 | HepG2 | liver: | n/a | n/a |
4 | FOXA1 | chr6:132855647-132856034 | HepG2 | liver: | n/a | n/a |
5 | NR2F2 | chr6:132855770-132856063 | HepG2 | liver: | n/a | n/a |
6 | FOXA2 | chr6:132855731-132856004 | HepG2 | liver: | n/a | n/a |
7 | JUND | chr6:132855747-132856034 | HepG2 | liver: | n/a | n/a |
8 | RXRA | chr6:132855662-132856042 | HepG2 | liver: | n/a | n/a |
9 | EP300 | chr6:132855654-132856038 | HepG2 | liver: | n/a | n/a |
10 | EP300 | chr6:132855732-132856127 | HepG2 | liver: | n/a | n/a |
11 | HNF4A | chr6:132855733-132856076 | HepG2 | liver: | n/a | n/a |
12 | SP1 | chr6:132855593-132856100 | HepG2 | liver: | n/a | n/a |
13 | SETDB1 | chr6:132855296-132856107 | U2OS | brain: | n/a | n/a |
14 | NR2F2 | chr6:132855770-132856026 | HepG2 | liver: | n/a | n/a |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:132855902..132859597-chr6:133135974..133139810,3 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
TAAR9 | TF binding region |
ENSG00000200534 | Chromatin interaction |
ENSG00000221500 | Chromatin interaction |
ENSG00000206754 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11758170 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12195306 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12209085 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12210154 | 0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061384 | 0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2066075 | 0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2066076 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2066077 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2153171 | 0.91[ASN][1000 genomes] |
rs2153178 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs58924219 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6569807 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6918805 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7743835 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7763434 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9321350 | 0.80[AMR][1000 genomes] |
rs9402425 | 0.80[AMR][1000 genomes] |
rs9483478 | 0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9493355 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9493360 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9493361 | 0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs9493362 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9493363 | 0.93[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs9493364 | 0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs9493365 | 0.91[EUR][1000 genomes] |
rs9493366 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9493367 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532069 | chr6:132776411-133462292 | Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 90 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:132855800-132856400 | Enhancers | HepG2 | liver |