Variant report

Variant	rs580585
Chromosome Location	chr3:94205768-94205769
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs11358995	0.91[EUR][1000 genomes]
rs12696211	0.91[EUR][1000 genomes]
rs12696217	0.90[EUR][1000 genomes]
rs13066412	0.89[EUR][1000 genomes]
rs13071621	0.89[EUR][1000 genomes]
rs13086509	0.90[EUR][1000 genomes]
rs13086687	0.90[EUR][1000 genomes]
rs13319500	0.85[EUR][1000 genomes]
rs13327303	0.90[EUR][1000 genomes]
rs1352463	0.90[EUR][1000 genomes]
rs1352467	0.85[EUR][1000 genomes]
rs1352468	0.85[EUR][1000 genomes]
rs1352469	0.84[EUR][1000 genomes]
rs1463688	0.85[EUR][1000 genomes]
rs1488774	0.85[EUR][1000 genomes]
rs1488790	0.85[EUR][1000 genomes]
rs1492009	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1688341	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1906648	0.85[EUR][1000 genomes]
rs1948183	0.86[EUR][1000 genomes]
rs4116	0.91[EUR][1000 genomes]
rs4323005	0.90[EUR][1000 genomes]
rs4346544	0.90[EUR][1000 genomes]
rs4428183	0.91[EUR][1000 genomes]
rs4575898	0.90[EUR][1000 genomes]
rs4599310	0.90[EUR][1000 genomes]
rs4626098	0.90[EUR][1000 genomes]
rs472026	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs479147	0.88[EUR][1000 genomes]
rs479882	0.88[EUR][1000 genomes]
rs480171	0.91[EUR][1000 genomes]
rs480907	0.90[EUR][1000 genomes]
rs483898	0.91[EUR][1000 genomes]
rs483921	0.91[EUR][1000 genomes]
rs4857116	0.85[EUR][1000 genomes]
rs4857117	0.85[EUR][1000 genomes]
rs4857118	0.85[EUR][1000 genomes]
rs4857449	0.85[EUR][1000 genomes]
rs4857450	0.85[EUR][1000 genomes]
rs4857451	0.85[EUR][1000 genomes]
rs495044	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs496227	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs497977	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs498902	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs499348	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs499845	0.91[EUR][1000 genomes]
rs501736	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs502484	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs507680	0.91[EUR][1000 genomes]
rs508575	0.90[EUR][1000 genomes]
rs511425	0.90[EUR][1000 genomes]
rs522161	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs525407	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs535230	0.91[EUR][1000 genomes]
rs538035	0.91[EUR][1000 genomes]
rs540867	0.91[EUR][1000 genomes]
rs548064	0.91[EUR][1000 genomes]
rs561209	0.91[EUR][1000 genomes]
rs567690	0.91[EUR][1000 genomes]
rs571833	0.91[EUR][1000 genomes]
rs571837	0.91[EUR][1000 genomes]
rs571949	0.91[EUR][1000 genomes]
rs574850	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs577311	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6441155	0.85[EUR][1000 genomes]
rs6768467	0.90[EUR][1000 genomes]
rs6773384	0.85[EUR][1000 genomes]
rs6788944	0.84[EUR][1000 genomes]
rs6799700	0.90[EUR][1000 genomes]
rs7621725	0.90[EUR][1000 genomes]
rs7632092	0.90[EUR][1000 genomes]
rs7638729	0.90[EUR][1000 genomes]
rs7643204	0.90[EUR][1000 genomes]
rs9290298	0.85[EUR][1000 genomes]
rs9290304	0.85[EUR][1000 genomes]
rs9290305	0.85[EUR][1000 genomes]
rs9290309	0.85[EUR][1000 genomes]
rs9813962	0.85[EUR][1000 genomes]
rs9832797	0.85[EUR][1000 genomes]
rs9835892	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9847601	0.90[EUR][1000 genomes]
rs9847703	0.91[EUR][1000 genomes]
rs9847873	0.90[EUR][1000 genomes]
rs9850669	0.83[EUR][1000 genomes]
rs9857736	0.85[EUR][1000 genomes]
rs9859318	0.90[EUR][1000 genomes]
rs9862108	0.90[EUR][1000 genomes]
rs9862366	0.85[EUR][1000 genomes]
rs9862859	0.90[EUR][1000 genomes]
rs9862924	0.91[EUR][1000 genomes]
rs9866100	0.91[EUR][1000 genomes]
rs9867789	0.84[EUR][1000 genomes]
rs9869466	0.90[EUR][1000 genomes]
rs9869892	0.91[EUR][1000 genomes]
rs9869898	0.91[EUR][1000 genomes]
rs9870578	0.90[EUR][1000 genomes]
rs987204	0.86[EUR][1000 genomes]
rs9873720	0.90[EUR][1000 genomes]
rs9875595	0.85[EUR][1000 genomes]
rs9990179	0.85[EUR][1000 genomes]
rs9990211	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869241	chr3:93527675-94504491	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv998173	chr3:93575084-94427403	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv536644	chr3:93575084-94427403	Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1008711	chr3:93575284-94427264	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv536646	chr3:93575284-94427264	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv491829	chr3:93575285-94427263	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv1004176	chr3:93654100-94502551	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv877162	chr3:93779664-94278078	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1000265	chr3:94012384-94259057	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv536650	chr3:94012384-94259057	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv997698	chr3:94030474-94212738	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv536651	chr3:94030474-94212738	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv834765	chr3:94116586-94321775	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:94201200-94207000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:94205400-94206800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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