Variant report

Variant	rs12334299
Chromosome Location	chr8:92257659-92257660
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	CEBPB	chr8:92257500-92257831	IMR90	lung:	n/a	chr8:92257654-92257663 chr8:92257652-92257665 chr8:92257654-92257663 chr8:92257653-92257664 chr8:92257654-92257663
2	CEBPB	chr8:92257537-92257915	MCF-7	breast:	n/a	chr8:92257654-92257663 chr8:92257652-92257665 chr8:92257654-92257663 chr8:92257653-92257664 chr8:92257654-92257663
3	CEBPB	chr8:92257503-92257828	H1-hESC	embryonic stem cell:	n/a	chr8:92257654-92257663 chr8:92257652-92257665 chr8:92257654-92257663 chr8:92257653-92257664 chr8:92257654-92257663
4	CEBPB	chr8:92257496-92257844	A549	lung:	n/a	chr8:92257654-92257663 chr8:92257652-92257665 chr8:92257654-92257663 chr8:92257653-92257664 chr8:92257654-92257663
5	CEBPB	chr8:92257487-92257830	HepG2	liver:	n/a	chr8:92257654-92257663 chr8:92257652-92257665 chr8:92257654-92257663 chr8:92257653-92257664 chr8:92257654-92257663
6	CEBPB	chr8:92257480-92257840	K562	blood:	n/a	chr8:92257654-92257663 chr8:92257652-92257665 chr8:92257654-92257663 chr8:92257653-92257664 chr8:92257654-92257663

Variant related genes	Relation type
SLC26A7	TF binding region

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10086690	0.82[CHB][hapmap]
rs10087080	0.82[CHB][hapmap]
rs10087372	0.82[CHB][hapmap]
rs10088008	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10089490	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10091010	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10091041	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10091616	0.82[CHB][hapmap]
rs10094031	0.82[JPT][hapmap]
rs10102397	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10105201	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10105880	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10108620	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10110426	1.00[CHB][hapmap]
rs10111757	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10112520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10113205	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10113232	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10113395	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10282965	1.00[CHB][hapmap]
rs10956798	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12334426	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs28475339	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28539046	0.96[ASN][1000 genomes]
rs28539271	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3210518	1.00[JPT][hapmap]
rs3808377	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4609161	1.00[JPT][hapmap]
rs62526735	0.96[ASN][1000 genomes]
rs62526740	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62526742	0.96[ASN][1000 genomes]
rs62527422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62527424	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62527425	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7005525	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7007552	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7009676	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92249400-92260400	Weak transcription	Fetal Lung	lung

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