Variant report

Variant	rs11466573
Chromosome Location	chr1:92262306-92262307
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1017956	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs1017957	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs10783036	0.96[CEU][hapmap];0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10783037	0.96[CEU][hapmap];0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10783040	0.85[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs10874941	0.87[ASN][1000 genomes]
rs10874981	0.96[CEU][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11165496	0.90[ASN][1000 genomes]
rs11165532	1.00[CEU][hapmap];0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1192530	0.90[ASN][1000 genomes]
rs12756024	0.89[ASN][1000 genomes]
rs1411276	0.86[ASN][1000 genomes]
rs1473486	0.85[ASN][1000 genomes]
rs1473488	0.86[ASN][1000 genomes]
rs1473767	0.86[ASN][1000 genomes]
rs2046739	0.82[EUR][1000 genomes]
rs2129975	0.96[CEU][hapmap];0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2171584	0.86[ASN][1000 genomes]
rs2297142	0.86[ASN][1000 genomes]
rs2489190	0.89[EUR][1000 genomes]
rs2634031	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs2799537	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs4658113	0.89[ASN][1000 genomes]
rs4658268	0.89[ASN][1000 genomes]
rs4658275	0.96[CEU][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs5019497	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6604054	0.89[ASN][1000 genomes]
rs6604055	0.88[ASN][1000 genomes]
rs6604056	1.00[CEU][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6678564	0.86[ASN][1000 genomes]
rs6683840	0.89[ASN][1000 genomes]
rs6691098	0.86[ASN][1000 genomes]
rs7530883	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats 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	14 gene(s)	inside rSNPs	diseases
2	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
19	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92248200-92268800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr1:92248600-92262800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:92248600-92268800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:92249200-92263800	Weak transcription	Aorta	Aorta
5	chr1:92250400-92263800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr1:92253200-92263600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:92254000-92269400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr1:92257600-92264000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:92257600-92279400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:92257800-92262800	Weak transcription	Lung	lung
11	chr1:92257800-92269600	Weak transcription	A549	lung
12	chr1:92258000-92262800	Weak transcription	Spleen	Spleen
13	chr1:92258000-92263800	Weak transcription	Esophagus	oesophagus
14	chr1:92258000-92264600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr1:92258000-92268400	Weak transcription	Fetal Thymus	thymus
16	chr1:92258200-92263800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr1:92258200-92269400	Weak transcription	Hela-S3	cervix
18	chr1:92258400-92264000	Weak transcription	Pancreas	Pancrea
19	chr1:92258400-92264400	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr1:92258400-92264600	Weak transcription	Fetal Intestine Large	intestine
21	chr1:92258400-92271400	Weak transcription	Fetal Intestine Small	intestine
22	chr1:92258600-92262600	Weak transcription	Right Ventricle	heart
23	chr1:92258600-92263000	Weak transcription	Brain Angular Gyrus	brain
24	chr1:92258600-92263600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:92258600-92263600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr1:92258600-92263600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr1:92258600-92263800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:92258600-92263800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr1:92258600-92263800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:92258600-92263800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr1:92258600-92264000	Weak transcription	Brain Anterior Caudate	brain
32	chr1:92258600-92264600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:92258600-92268600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:92258600-92270000	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr1:92258800-92263600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:92258800-92272400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr1:92259000-92262600	Weak transcription	Ovary	ovary
38	chr1:92259000-92263800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:92259000-92264400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr1:92259600-92263000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:92260000-92263000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr1:92260200-92263200	Genic enhancers	NHDF-Ad	bronchial
43	chr1:92260400-92271200	Strong transcription	HepG2	liver
44	chr1:92260600-92264400	Enhancers	Fetal Heart	heart
45	chr1:92260800-92263400	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr1:92260800-92268800	Weak transcription	Small Intestine	intestine
47	chr1:92261000-92263000	Strong transcription	Liver	Liver
48	chr1:92261200-92263200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr1:92261600-92262400	Strong transcription	Placenta	Placenta
50	chr1:92261600-92262800	Strong transcription	Adipose Nuclei	Adipose

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