Variant report

Variant	rs12210860
Chromosome Location	chr6:117950691-117950692
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr6:117950257-117950745	HepG2	liver:	n/a	n/a
2	FOXA1	chr6:117950216-117950713	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
NEPNP	TF binding region

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10456911	1.00[ASN][1000 genomes]
rs10456912	1.00[ASN][1000 genomes]
rs10457319	1.00[ASN][1000 genomes]
rs10457320	1.00[ASN][1000 genomes]
rs10484301	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10872154	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11153674	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11758156	1.00[ASN][1000 genomes]
rs12192117	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12193035	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12194014	1.00[ASN][1000 genomes]
rs12196716	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12197399	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12200953	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12205852	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12208894	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12209222	1.00[ASN][1000 genomes]
rs12209927	1.00[ASN][1000 genomes]
rs12215701	1.00[ASN][1000 genomes]
rs17637404	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17818735	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2134088	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs41291926	1.00[ASN][1000 genomes]
rs56020204	1.00[ASN][1000 genomes]
rs72965600	1.00[ASN][1000 genomes]
rs72967203	1.00[ASN][1000 genomes]
rs72967214	1.00[ASN][1000 genomes]
rs916305	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs929059	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9320605	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9481727	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9489220	1.00[ASN][1000 genomes]
rs9688605	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9766117	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9766656	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9766945	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9766959	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs9767675	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117943600-117951400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:117949400-117951000	Enhancers	Liver	Liver
3	chr6:117949800-117951000	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr6:117950000-117950800	Enhancers	HepG2	liver
5	chr6:117950200-117950800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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