Variant report

Variant	rs11039205
Chromosome Location	chr11:5851468-5851469
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1032648	0.88[AMR][1000 genomes]
rs11039100	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039101	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039110	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039115	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039116	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039117	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039118	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039120	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039121	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11039164	0.92[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12361754	0.87[AMR][1000 genomes]
rs12362071	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12362696	0.87[AMR][1000 genomes]
rs12363853	0.89[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12363855	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12366070	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12791839	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12792672	0.92[AMR][1000 genomes]
rs12792905	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12792952	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12793142	0.85[AMR][1000 genomes]
rs12796660	0.92[AMR][1000 genomes]
rs12798822	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12798823	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1470872	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1470873	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34037040	0.92[AMR][1000 genomes]
rs34123108	0.92[AMR][1000 genomes]
rs34161300	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34286221	0.92[AMR][1000 genomes]
rs34818213	0.92[AMR][1000 genomes]
rs34930440	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35466594	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35746872	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35863959	0.92[AMR][1000 genomes]
rs35863965	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35990969	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4280027	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4319539	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4474469	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs61875914	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs61875915	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs72896130	0.92[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	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
3	nsv1053414	chr11:5612989-6030212	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	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
5	nsv553273	chr11:5639873-5871831	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	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
7	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
8	nsv553277	chr11:5722948-6010075	Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
9	esv1843296	chr11:5730377-5970717	Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	esv2758255	chr11:5730377-5970717	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
11	esv2759801	chr11:5730377-6007613	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
12	nsv832058	chr11:5747594-5926814	Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
13	nsv896952	chr11:5832191-5893376	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
14	nsv971927	chr11:5842082-5988665	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv1043316	chr11:5847076-5887925	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
16	nsv1042501	chr11:5850871-5887925	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	5 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	chr11:5847800-5852600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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