Variant report

Variant	rs7957797
Chromosome Location	chr12:85871974-85871975
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10746344	0.86[ASN][1000 genomes]
rs10746346	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10746347	0.91[ASN][1000 genomes]
rs10779161	0.97[ASN][1000 genomes]
rs10779164	0.94[ASN][1000 genomes]
rs10779167	0.92[ASN][1000 genomes]
rs10779168	0.92[ASN][1000 genomes]
rs10779169	0.92[ASN][1000 genomes]
rs10779170	0.92[ASN][1000 genomes]
rs10779173	0.91[ASN][1000 genomes]
rs10779180	0.85[ASN][1000 genomes]
rs10779181	0.84[ASN][1000 genomes]
rs10779182	0.82[ASN][1000 genomes]
rs10862979	0.93[ASN][1000 genomes]
rs10862990	0.92[ASN][1000 genomes]
rs10862991	0.91[ASN][1000 genomes]
rs10862993	0.92[ASN][1000 genomes]
rs10862999	0.92[ASN][1000 genomes]
rs10863000	0.92[ASN][1000 genomes]
rs10863007	0.91[ASN][1000 genomes]
rs10863008	0.91[ASN][1000 genomes]
rs10863032	0.82[ASN][1000 genomes]
rs11116807	0.97[ASN][1000 genomes]
rs11116832	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11116833	0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11116930	0.89[ASN][1000 genomes]
rs11116934	0.85[ASN][1000 genomes]
rs11116935	0.85[ASN][1000 genomes]
rs11831266	0.91[ASN][1000 genomes]
rs11835161	0.84[ASN][1000 genomes]
rs12578708	0.86[ASN][1000 genomes]
rs1398440	0.97[ASN][1000 genomes]
rs1398442	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1870933	0.90[ASN][1000 genomes]
rs1870935	0.90[ASN][1000 genomes]
rs2199508	0.83[ASN][1000 genomes]
rs2199511	0.84[ASN][1000 genomes]
rs2199512	0.84[ASN][1000 genomes]
rs2199513	0.86[ASN][1000 genomes]
rs2199516	0.91[ASN][1000 genomes]
rs2199517	0.91[ASN][1000 genomes]
rs2199518	0.91[ASN][1000 genomes]
rs2219711	0.84[ASN][1000 genomes]
rs2405248	0.90[ASN][1000 genomes]
rs2405254	0.86[ASN][1000 genomes]
rs2405256	0.84[ASN][1000 genomes]
rs2405257	0.82[ASN][1000 genomes]
rs4761063	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4897817	0.85[ASN][1000 genomes]
rs4897825	0.84[ASN][1000 genomes]
rs6419420	0.98[ASN][1000 genomes]
rs6419421	0.92[ASN][1000 genomes]
rs6539899	0.92[ASN][1000 genomes]
rs6539901	0.85[ASN][1000 genomes]
rs6539902	0.84[ASN][1000 genomes]
rs7133064	0.84[ASN][1000 genomes]
rs7133855	0.92[ASN][1000 genomes]
rs7134486	0.92[ASN][1000 genomes]
rs7136236	0.89[ASN][1000 genomes]
rs7295445	0.84[ASN][1000 genomes]
rs7297262	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7302629	0.84[ASN][1000 genomes]
rs7303316	0.92[ASN][1000 genomes]
rs7304475	0.82[ASN][1000 genomes]
rs7316167	0.86[ASN][1000 genomes]
rs7485084	0.92[ASN][1000 genomes]
rs7485590	0.92[ASN][1000 genomes]
rs7486767	0.92[ASN][1000 genomes]
rs7487599	0.98[ASN][1000 genomes]
rs7955601	0.82[ASN][1000 genomes]
rs7966898	0.80[ASN][1000 genomes]
rs7973153	0.82[ASN][1000 genomes]
rs7973323	0.92[ASN][1000 genomes]
rs7977259	0.92[ASN][1000 genomes]
rs898986	0.89[ASN][1000 genomes]
rs9788015	0.91[ASN][1000 genomes]
rs9788074	0.91[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	esv1792335	chr12:85321249-86003609	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv817242	chr12:85622245-86069213	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1054573	chr12:85658602-86235433	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1035600	chr12:85661373-86235433	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1053044	chr12:85843030-85942504	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1036617	chr12:85855093-86010549	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85863000-85873000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:85863000-85874800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:85864200-85872000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr12:85871600-85872000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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