Variant report

Variant	rs11823761
Chromosome Location	chr11:71315598-71315599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11821792	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11822897	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11823917	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11824522	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11827597	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1806494	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1815778	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2077324	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28516412	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28694042	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28859366	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35006055	0.82[EUR][1000 genomes]
rs4328237	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56334837	0.96[EUR][1000 genomes]
rs56408192	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58201438	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58813746	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59308270	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs60055671	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs60062165	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs60905863	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61333469	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6592241	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6592242	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6592243	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6592244	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6592245	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7109650	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7111892	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7114767	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7119660	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7127788	0.96[EUR][1000 genomes]
rs7128030	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7925528	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7929273	0.91[EUR][1000 genomes]
rs7936597	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7951132	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9666675	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9667234	0.96[EUR][1000 genomes]
rs9735265	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9736187	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	esv3372246	chr11:71223101-71435819	Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1043207	chr11:71293875-71442666	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1037088	chr11:71293875-71538991	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	esv3527986	chr11:71298409-71620955	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
6	esv3527987	chr11:71298409-71620955	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	nsv1036258	chr11:71299175-71523551	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	nsv1041027	chr11:71299175-71527896	Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv1051879	chr11:71299175-71536860	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
10	nsv1044041	chr11:71299175-71538991	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	esv2761682	chr11:71299175-71619923	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
12	nsv555403	chr11:71301189-71430470	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	esv3369271	chr11:71307946-71334603	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv972040	chr11:71315526-71330518	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS	TF binding region CpG island	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	chr11:71315200-71316000	Enhancers	Fetal Thymus	thymus

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