Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11154605	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11154606	0.91[EUR][1000 genomes]
rs11751010	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11753133	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1497890	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1605604	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17059459	0.82[EUR][1000 genomes]
rs17059460	0.82[EUR][1000 genomes]
rs17059464	0.82[EUR][1000 genomes]
rs17059550	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1988279	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2030022	0.83[AFR][1000 genomes]
rs4895893	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4897458	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4897462	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4897467	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62422290	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62425266	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6914815	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6937163	0.86[ASN][1000 genomes]
rs7747747	0.81[EUR][1000 genomes]
rs9492699	0.82[EUR][1000 genomes]
rs9492704	0.82[EUR][1000 genomes]
rs9492710	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9492712	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs994211	0.82[EUR][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	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv830806	chr6:130938330-131107137	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv604664	chr6:131004998-131115817	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1025019	chr6:131074711-131116070	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv604665	chr6:131077027-131115817	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv604666	chr6:131078180-131122295	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131099800-131103800	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr6:131101400-131105600	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:131101600-131104000	Weak transcription	Fetal Stomach	stomach

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