Variant report

Variant	rs1809433
Chromosome Location	chr12:37891448-37891449
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 88 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs11169903	0.81[AFR][1000 genomes]
rs11829077	0.87[AFR][1000 genomes]
rs11829343	0.84[AFR][1000 genomes]
rs11829811	0.84[AFR][1000 genomes]
rs11830074	0.81[AFR][1000 genomes]
rs11830953	0.81[AFR][1000 genomes]
rs11831020	0.81[AFR][1000 genomes]
rs11831022	0.81[AFR][1000 genomes]
rs11832208	0.87[AFR][1000 genomes]
rs11832757	0.87[AFR][1000 genomes]
rs11834349	0.87[AFR][1000 genomes]
rs11834375	0.87[AFR][1000 genomes]
rs11835115	0.87[AFR][1000 genomes]
rs11838038	0.84[AFR][1000 genomes]
rs12099458	0.87[AFR][1000 genomes]
rs12099748	0.82[AFR][1000 genomes]
rs12099754	0.87[AFR][1000 genomes]
rs12099828	0.87[AFR][1000 genomes]
rs36091545	0.84[AFR][1000 genomes]
rs4002695	1.00[AFR][1000 genomes]
rs55694285	0.87[AFR][1000 genomes]
rs55725952	0.87[AFR][1000 genomes]
rs55917139	0.87[AFR][1000 genomes]
rs56036406	0.87[AFR][1000 genomes]
rs56156183	0.84[AFR][1000 genomes]
rs56244344	0.87[AFR][1000 genomes]
rs56321587	0.87[AFR][1000 genomes]
rs56665125	0.87[AFR][1000 genomes]
rs56981354	0.87[AFR][1000 genomes]
rs57631917	0.87[AFR][1000 genomes]
rs57788299	0.87[AFR][1000 genomes]
rs58020099	0.90[AFR][1000 genomes]
rs58120371	0.84[AFR][1000 genomes]
rs58690601	0.81[AFR][1000 genomes]
rs58781657	0.87[AFR][1000 genomes]
rs58811384	0.87[AFR][1000 genomes]
rs58893539	0.87[AFR][1000 genomes]
rs59000856	0.87[AFR][1000 genomes]
rs59270476	0.87[AFR][1000 genomes]
rs59308288	0.87[AFR][1000 genomes]
rs59420277	0.84[AFR][1000 genomes]
rs59640272	0.87[AFR][1000 genomes]
rs59716634	0.87[AFR][1000 genomes]
rs59887419	0.81[AFR][1000 genomes]
rs60676502	0.87[AFR][1000 genomes]
rs60683175	0.87[AFR][1000 genomes]
rs60866126	0.87[AFR][1000 genomes]
rs61105337	0.87[AFR][1000 genomes]
rs61120955	0.87[AFR][1000 genomes]
rs61394467	0.81[AFR][1000 genomes]
rs74072574	0.87[AFR][1000 genomes]
rs74074103	0.87[AFR][1000 genomes]
rs74074104	0.87[AFR][1000 genomes]
rs74076055	0.87[AFR][1000 genomes]
rs74076071	0.87[AFR][1000 genomes]
rs74076074	0.87[AFR][1000 genomes]
rs74076077	0.87[AFR][1000 genomes]
rs74076079	0.87[AFR][1000 genomes]
rs74076081	0.87[AFR][1000 genomes]
rs74076082	0.87[AFR][1000 genomes]
rs9705423	0.84[AFR][1000 genomes]
rs9705424	0.84[AFR][1000 genomes]
rs9705427	0.84[AFR][1000 genomes]
rs9706078	0.87[AFR][1000 genomes]
rs9706257	0.84[AFR][1000 genomes]
rs9706261	0.81[AFR][1000 genomes]
rs9706540	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428278	chr12:37856695-38153429	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv976600	chr12:37856695-38447701	ZNF genes & repeats Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1037979	chr12:37857751-37913525	Enhancers	n/a	n/a	inside rSNPs	diseases
4	nsv1049436	chr12:37857751-37976960	Enhancers ZNF genes & repeats Active TSS Weak transcription	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1048872	chr12:37857751-37987714	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1053368	chr12:37857751-38014006	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1038702	chr12:37857751-38034346	ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1046126	chr12:37857751-38054151	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1038938	chr12:37857751-38081271	Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv1054862	chr12:37857751-38108041	ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1043650	chr12:37857751-38169729	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1048715	chr12:37857751-38283657	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv1043459	chr12:37857751-38662460	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
14	nsv1050718	chr12:37857751-38757302	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
15	nsv558346	chr12:37857899-38145285	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv898972	chr12:37857899-38719455	ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv558347	chr12:37860597-37926452	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
18	nsv558348	chr12:37860597-38424982	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
19	nsv826329	chr12:37864282-37936522	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
20	nsv558349	chr12:37870474-38187236	ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
21	esv2754312	chr12:37890833-38424933	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr12:37891400-37892600	Enhancers	Dnd41	blood

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