Variant report

Variant	rs2422361
Chromosome Location	chr11:36756254-36756255
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10501162	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836594	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10836595	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836596	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836597	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836598	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836599	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836600	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836601	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836603	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836604	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10836605	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033765	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11033766	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033768	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033769	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033770	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11033774	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11033775	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033776	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11033779	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033781	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11033782	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12223727	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12225581	0.88[EUR][1000 genomes]
rs12225583	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12226823	0.83[EUR][1000 genomes]
rs12271535	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12271541	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12276665	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12276715	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12279194	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12280907	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12281077	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12284660	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12294055	0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12294160	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12294236	0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1401289	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1401290	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1401291	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1518745	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1589177	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16929349	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1996536	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1996537	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2139137	0.90[EUR][1000 genomes]
rs2139138	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2176594	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2901722	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4332497	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4332498	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4582952	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4755456	0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4755457	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4755459	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756336	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4756337	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4756338	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756339	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756340	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756341	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4756342	0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55877156	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56111224	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61078470	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61877683	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61877684	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61877685	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61877686	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61877687	0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72947155	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7929934	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7933480	0.99[EUR][1000 genomes];0.94[ASN][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	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers 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	18 gene(s)	inside rSNPs	diseases
3	nsv832123	chr11:36582872-36757443	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv467792	chr11:36624187-36898373	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv554005	chr11:36624187-36898373	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv467793	chr11:36632515-37171833	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv554006	chr11:36632515-37171833	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1047073	chr11:36711638-36812910	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1041508	chr11:36711638-36815367	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1043391	chr11:36711638-36817144	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv554007	chr11:36711834-36825618	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv11137	chr11:36730247-36788022	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	esv2761663	chr11:36730335-36786817	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 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	chr11:36746800-36759600	Weak transcription	Thymus	Thymus

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