Variant report

Variant	rs7943304
Chromosome Location	chr11:6114226-6114227
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:79)

rs_ID	r²[population]
rs10769656	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10769657	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10769658	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10769659	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs10839476	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10839477	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10839478	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10839479	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs10839489	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10839491	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10839509	0.83[AFR][1000 genomes]
rs10839510	0.83[AFR][1000 genomes]
rs10839512	0.83[AFR][1000 genomes]
rs10839513	0.83[AFR][1000 genomes]
rs11040648	0.80[EUR][1000 genomes]
rs11040649	0.80[EUR][1000 genomes]
rs11040650	0.80[EUR][1000 genomes]
rs11040652	0.80[EUR][1000 genomes]
rs11040653	0.80[EUR][1000 genomes]
rs11040709	0.82[EUR][1000 genomes]
rs11040713	0.82[EUR][1000 genomes]
rs11040714	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11040715	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs11040717	0.82[EUR][1000 genomes]
rs11040718	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11040741	0.83[AFR][1000 genomes]
rs11511999	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12360715	0.83[AFR][1000 genomes]
rs12803982	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs12806233	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1462982	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1599689	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs1599690	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34481020	0.83[AFR][1000 genomes]
rs34682998	0.83[AFR][1000 genomes]
rs34814525	0.81[AFR][1000 genomes]
rs35261017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35368155	0.83[AFR][1000 genomes]
rs35515581	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35682479	0.83[AFR][1000 genomes]
rs35829351	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs4362124	0.80[EUR][1000 genomes]
rs4604856	0.80[EUR][1000 genomes]
rs4758080	0.80[EUR][1000 genomes]
rs4758379	0.80[EUR][1000 genomes]
rs4758384	0.90[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs4758385	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs4758386	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs5005636	0.83[AFR][1000 genomes]
rs5005637	0.83[AFR][1000 genomes]
rs5005639	0.83[AFR][1000 genomes]
rs5005640	0.83[AFR][1000 genomes]
rs5005642	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5005643	0.83[AFR][1000 genomes]
rs6578736	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs6578737	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7104448	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7106139	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7106179	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7111479	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7114613	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7114866	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7117092	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7117349	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7122336	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7122340	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7123409	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7929863	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs7929888	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7932413	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7932884	0.82[EUR][1000 genomes]
rs7935717	0.87[AFR][1000 genomes]
rs7935845	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7941058	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7943059	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7943285	0.88[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7946421	0.87[AFR][1000 genomes]
rs7952121	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7952132	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553241	chr11:5506034-6203685	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv530216	chr11:5614439-6468232	Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1036389	chr11:5695451-6177680	Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
4	nsv540943	chr11:5695451-6177680	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
5	nsv1047794	chr11:6003428-6116105	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	esv19708	chr11:6076999-6117545	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv10302	chr11:6104402-6121639	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
8	nsv553353	chr11:6112857-6117526	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:6112800-6117200	Weak transcription	Fetal Heart	heart

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