Variant report

Variant	rs28795368
Chromosome Location	chr8:39125404-39125405
allele	G/T
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	EP300	chr8:39125282-39125619	HepG2	liver:	n/a	n/a
2	TEAD4	chr8:39125204-39125544	H1-hESC	embryonic stem cell:	n/a	n/a
3	FOXA1	chr8:39125191-39125635	HepG2	liver:	n/a	n/a
4	TEAD4	chr8:39125143-39125523	H1-hESC	embryonic stem cell:	n/a	n/a
5	FOXA2	chr8:39125308-39125550	HepG2	liver:	n/a	n/a
6	HNF4A	chr8:39125371-39125592	HepG2	liver:	n/a	n/a
7	FOXA1	chr8:39125313-39125567	HepG2	liver:	n/a	n/a
8	TEAD4	chr8:39125145-39125553	HepG2	liver:	n/a	n/a
9	FOSL2	chr8:39125266-39125545	HepG2	liver:	n/a	n/a
10	FOXA1	chr8:39125281-39125572	HepG2	liver:	n/a	n/a
11	FOXA1	chr8:39125229-39125716	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
ADAM32	TF binding region

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10088174	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10093393	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10808920	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10958543	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11776234	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11777253	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11782591	0.81[EUR][1000 genomes]
rs11786406	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12675132	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12679074	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12682638	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28460316	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28649569	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28788037	0.81[EUR][1000 genomes]
rs4128223	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4316117	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4515515	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4585713	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4733912	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4733992	0.81[EUR][1000 genomes]
rs4733994	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55759907	0.81[EUR][1000 genomes]
rs55817221	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56093547	0.81[EUR][1000 genomes]
rs57822948	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58036010	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6474126	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6988280	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989252	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7001103	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7013701	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7016661	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72500200	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73606793	0.81[EUR][1000 genomes]
rs73608630	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73608634	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73608636	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7464434	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7816763	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7843723	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7843946	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015907	chr8:38967169-39718559	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv539550	chr8:38967169-39718559	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1027443	chr8:38993423-39181079	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv539551	chr8:38993423-39181079	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv428198	chr8:39069309-39405724	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1019752	chr8:39087542-39371410	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv1798122	chr8:39101565-39405724	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv1809741	chr8:39101565-39405724	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv1815710	chr8:39101565-39405724	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv1827982	chr8:39101565-39405724	ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv1829387	chr8:39101565-39405724	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv1845167	chr8:39101565-39405724	Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	esv3421887	chr8:39103844-39132832	ZNF genes & repeats Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	esv1845068	chr8:39120649-39452805	Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39124600-39125600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:39125200-39125800	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links