Variant report

Variant	rs4570568
Chromosome Location	chr11:8203892-8203893
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10743053	0.85[EUR][1000 genomes]
rs10743054	0.85[EUR][1000 genomes]
rs10743055	0.85[EUR][1000 genomes]
rs11041785	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11041791	0.83[ASN][1000 genomes]
rs11041792	0.84[ASN][1000 genomes]
rs12222717	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12278538	0.83[ASN][1000 genomes]
rs12802958	0.85[ASN][1000 genomes]
rs12808387	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1528125	0.84[EUR][1000 genomes]
rs1569127	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1918847	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1970880	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1997262	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35671424	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35727940	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4758305	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4758307	0.85[ASN][1000 genomes]
rs4758308	0.85[ASN][1000 genomes]
rs4758309	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4758310	0.86[ASN][1000 genomes]
rs55752700	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61527420	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7103334	0.85[EUR][1000 genomes]
rs7112519	0.84[ASN][1000 genomes]
rs7115706	0.84[ASN][1000 genomes]
rs7127259	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7127738	0.84[EUR][1000 genomes]
rs7479133	0.85[EUR][1000 genomes]
rs7479156	0.85[EUR][1000 genomes]
rs7479738	0.85[EUR][1000 genomes]
rs7481667	0.81[EUR][1000 genomes]
rs7481683	0.80[EUR][1000 genomes]
rs7481742	0.86[EUR][1000 genomes]
rs7481907	0.85[EUR][1000 genomes]
rs7931434	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7941224	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7952275	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829170	chr11:8068594-8216369	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv428249	chr11:8068594-8216369	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv896981	chr11:8152080-8227964	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1054339	chr11:8153582-8263173	Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv553443	chr11:8200216-8211920	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv1826805	chr11:8201022-8215751	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv1829890	chr11:8201022-8215751	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv553444	chr11:8201125-8215751	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv553445	chr11:8201305-8215853	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 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	chr11:8202600-8213800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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