Variant report

Variant	rs11980886
Chromosome Location	chr7:50165580-50165581
allele	A/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	BHLHE40	chr7:50165477-50165646	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
ZPBP	TF binding region

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10228836	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10235301	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10241289	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10250629	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10260654	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10267578	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11185600	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12667606	0.81[AFR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12672941	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12673071	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12718245	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12718246	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13241637	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1456906	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17133694	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17133709	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1870030	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1982535	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34733935	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34984574	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35254219	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35570047	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36129824	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3891340	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4092362	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4496918	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6943189	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7786619	0.80[ASN][1000 genomes]
rs7800478	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7805656	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs998928	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464444	chr7:49671882-50454736	Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv606897	chr7:49671883-50454736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv498090	chr7:49708644-50427714	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1020869	chr7:49712860-50457544	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv3367735	chr7:50163956-50166004	Inactive region	TF binding region	1 gene(s)	inside rSNPs	diseases
6	esv3437788	chr7:50164406-50165654	Inactive region	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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