Variant report

Variant	rs66625589
Chromosome Location	chr11:107703436-107703437
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10890764	1.00[EUR][1000 genomes]
rs11212379	0.86[EUR][1000 genomes]
rs11212383	0.91[EUR][1000 genomes]
rs11212389	1.00[EUR][1000 genomes]
rs11212390	1.00[EUR][1000 genomes]
rs11212391	1.00[EUR][1000 genomes]
rs11212392	1.00[EUR][1000 genomes]
rs11212393	1.00[EUR][1000 genomes]
rs11212394	1.00[EUR][1000 genomes]
rs11212395	1.00[EUR][1000 genomes]
rs11212396	1.00[EUR][1000 genomes]
rs11212397	1.00[EUR][1000 genomes]
rs11212398	1.00[EUR][1000 genomes]
rs11212400	1.00[EUR][1000 genomes]
rs12098896	1.00[EUR][1000 genomes]
rs12099368	1.00[EUR][1000 genomes]
rs12099420	0.82[EUR][1000 genomes]
rs12146456	1.00[EUR][1000 genomes]
rs12146459	1.00[EUR][1000 genomes]
rs12270982	0.91[EUR][1000 genomes]
rs12271120	1.00[EUR][1000 genomes]
rs12278904	1.00[EUR][1000 genomes]
rs12279264	0.95[EUR][1000 genomes]
rs12281160	1.00[EUR][1000 genomes]
rs12282500	0.97[ASN][1000 genomes]
rs12288093	1.00[EUR][1000 genomes]
rs12289394	0.94[ASN][1000 genomes]
rs12291200	1.00[EUR][1000 genomes]
rs12292050	1.00[EUR][1000 genomes]
rs12292254	1.00[EUR][1000 genomes]
rs12293650	1.00[EUR][1000 genomes]
rs503151	0.97[ASN][1000 genomes]
rs57429831	1.00[EUR][1000 genomes]
rs58124926	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58472728	0.97[ASN][1000 genomes]
rs59036211	1.00[EUR][1000 genomes]
rs60539601	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67596776	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7118580	1.00[EUR][1000 genomes]
rs7120382	0.86[EUR][1000 genomes]
rs72999546	0.86[EUR][1000 genomes]
rs73001540	1.00[EUR][1000 genomes]
rs73001542	0.81[EUR][1000 genomes]
rs73001547	1.00[EUR][1000 genomes]
rs73001550	1.00[EUR][1000 genomes]
rs73001554	1.00[EUR][1000 genomes]
rs73001562	1.00[EUR][1000 genomes]
rs73001563	1.00[EUR][1000 genomes]
rs73001566	1.00[EUR][1000 genomes]
rs73003327	1.00[EUR][1000 genomes]
rs73003344	1.00[EUR][1000 genomes]
rs73003346	1.00[EUR][1000 genomes]
rs73003355	1.00[EUR][1000 genomes]
rs73003360	1.00[EUR][1000 genomes]
rs73003382	1.00[EUR][1000 genomes]
rs73003384	1.00[EUR][1000 genomes]
rs73005370	0.95[EUR][1000 genomes]
rs73546814	0.90[ASN][1000 genomes]
rs73546826	0.97[ASN][1000 genomes]
rs73546873	0.97[ASN][1000 genomes]
rs9804577	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533794	chr11:107349817-108093259	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1039425	chr11:107468681-107895836	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv427899	chr11:107471544-107805894	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1049524	chr11:107540937-107954011	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1038581	chr11:107564274-107838386	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv898378	chr11:107580985-107847983	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv521771	chr11:107590335-107904646	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv1048938	chr11:107604473-107929950	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
9	nsv1035229	chr11:107653731-107717190	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv1052829	chr11:107686808-107725297	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv1045388	chr11:107686808-107733498	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	esv3417743	chr11:107699670-107725103	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107673400-107727800	Weak transcription	Primary B cells from cord blood	blood
2	chr11:107691200-107709600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:107696600-107711000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:107697200-107709800	Weak transcription	GM12878-XiMat	blood
5	chr11:107701400-107703800	Enhancers	HMEC	breast
6	chr11:107701400-107704000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:107701400-107704000	Enhancers	NHEK	skin
8	chr11:107701400-107704400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:107701600-107704400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:107701800-107703600	Enhancers	K562	blood
11	chr11:107702200-107709800	Weak transcription	A549	lung
12	chr11:107702200-107710600	Weak transcription	Stomach Mucosa	stomach
13	chr11:107702400-107710600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr11:107702400-107710800	Weak transcription	Gastric	stomach
15	chr11:107702800-107707200	Weak transcription	Duodenum Mucosa	Duodenum
16	chr11:107702800-107710600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:107703000-107703600	Enhancers	Esophagus	oesophagus
18	chr11:107703000-107704600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr11:107703000-107708800	Weak transcription	HUVEC	blood vessel
20	chr11:107703200-107703800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
21	chr11:107703200-107703800	Enhancers	HepG2	liver
22	chr11:107703200-107704200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:107703200-107705000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:107703200-107705800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr11:107703400-107703600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr11:107703400-107703600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr11:107703400-107704200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:107703400-107704200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:107703400-107704200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr11:107703400-107704400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr11:107703400-107705200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:107703400-107707200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links