Variant report

Variant	rs11020665
Chromosome Location	chr11:93891890-93891891
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10160353	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11020659	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11499643	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11603543	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11607757	0.91[EUR][1000 genomes]
rs12273690	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4593973	0.93[EUR][1000 genomes]
rs56157454	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56175344	0.91[EUR][1000 genomes]
rs57562692	0.95[EUR][1000 genomes]
rs6483298	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7117339	0.94[EUR][1000 genomes]
rs7129505	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72970792	0.95[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	nsv898183	chr11:93725384-93906735	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv898184	chr11:93741612-93969726	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1046092	chr11:93833446-93964452	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv898185	chr11:93851048-93927529	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv469980	chr11:93864321-93962121	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv468795	chr11:93864321-93964917	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv555966	chr11:93864321-93964917	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv517664	chr11:93866147-93913036	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93882400-93896800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr11:93882800-93895400	Weak transcription	Fetal Stomach	stomach
3	chr11:93883000-93906600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:93883200-93892600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr11:93883400-93906400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr11:93884000-93912800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr11:93884200-93895200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:93884400-93905400	Weak transcription	Right Ventricle	heart
9	chr11:93885200-93916200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr11:93885400-93899400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr11:93885400-93911200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr11:93885800-93897600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr11:93886000-93896600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:93886000-93896800	Weak transcription	Lung	lung
15	chr11:93886000-93903400	Weak transcription	HSMM	muscle
16	chr11:93886000-93905200	Weak transcription	HSMMtube	muscle
17	chr11:93886000-93913000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr11:93886200-93910800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:93886600-93913000	Weak transcription	K562	blood
20	chr11:93886800-93912800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr11:93887000-93911600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr11:93887400-93898800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr11:93887600-93894800	Weak transcription	NHLF	lung
24	chr11:93887600-93899400	Weak transcription	Fetal Lung	lung
25	chr11:93887600-93902000	Weak transcription	Gastric	stomach
26	chr11:93887600-93903800	Weak transcription	Left Ventricle	heart
27	chr11:93887600-93904600	Weak transcription	Aorta	Aorta
28	chr11:93887600-93907600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr11:93887600-93907800	Weak transcription	Colon Smooth Muscle	Colon
30	chr11:93887600-93908200	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr11:93887600-93908800	Weak transcription	Adipose Nuclei	Adipose
32	chr11:93887600-93910600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr11:93887600-93910800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr11:93887600-93911600	Weak transcription	Spleen	Spleen
35	chr11:93887800-93894600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr11:93887800-93895600	Weak transcription	Ovary	ovary
37	chr11:93887800-93899200	Weak transcription	Primary B cells from peripheral blood	blood
38	chr11:93887800-93904800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr11:93887800-93907800	Weak transcription	HMEC	breast
40	chr11:93887800-93908000	Weak transcription	NH-A	brain
41	chr11:93887800-93910800	Weak transcription	Liver	Liver
42	chr11:93888000-93892600	Weak transcription	Fetal Muscle Leg	muscle
43	chr11:93888000-93894800	Weak transcription	Fetal Intestine Small	intestine
44	chr11:93888000-93895600	Weak transcription	Fetal Intestine Large	intestine
45	chr11:93888000-93907200	Weak transcription	NHDF-Ad	bronchial
46	chr11:93889600-93899400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr11:93889600-93908600	Weak transcription	Stomach Smooth Muscle	stomach
48	chr11:93889800-93892000	Weak transcription	Fetal Brain Female	brain
49	chr11:93889800-93894800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr11:93889800-93895000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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