Variant report

Variant	rs2302262
Chromosome Location	chr11:64022814-64022815
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:64017311..64024506-chr11:64050135..64055747,10	MCF-7	breast:
2	chr11:64022032..64023751-chr11:64070140..64071822,2	MCF-7	breast:
3	chr11:62607453..62609584-chr11:64021907..64023770,2	K562	blood:
4	chr11:64020572..64023323-chr11:64085691..64088535,2	K562	blood:
5	chr11:64021477..64024375-chr11:64060158..64061742,2	MCF-7	breast:
6	chr11:63930758..63935103-chr11:64018023..64022943,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000002330	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000173264	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10128595	0.82[ASN][1000 genomes]
rs10128649	0.98[ASN][1000 genomes]
rs10556	1.00[ASN][1000 genomes]
rs10732887	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1124660	0.85[ASN][1000 genomes]
rs1207462	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs1213140	0.93[ASN][1000 genomes]
rs12271952	0.88[ASN][1000 genomes]
rs12281471	0.93[ASN][1000 genomes]
rs12283639	0.93[ASN][1000 genomes]
rs12287065	1.00[ASN][1000 genomes]
rs12574188	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs12575515	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs12575690	0.91[ASN][1000 genomes]
rs12577422	0.80[ASN][1000 genomes]
rs12577425	1.00[CHB][hapmap]
rs1468558	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17159027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1783518	0.89[CHB][hapmap];0.80[ASN][1000 genomes]
rs2154977	1.00[EUR][1000 genomes]
rs2232410	1.00[CHB][hapmap];0.82[JPT][hapmap];0.98[ASN][1000 genomes]
rs2282548	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs2286612	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2289572	0.91[ASN][1000 genomes]
rs28682946	0.82[ASN][1000 genomes]
rs320134	1.00[EUR][1000 genomes]
rs320136	1.00[EUR][1000 genomes]
rs3759056	0.93[ASN][1000 genomes]
rs3897565	1.00[EUR][1000 genomes]
rs41294376	0.91[ASN][1000 genomes]
rs41294424	0.82[ASN][1000 genomes]
rs473379	0.82[ASN][1000 genomes]
rs490720	0.82[ASN][1000 genomes]
rs4930167	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs493052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs494998	0.82[ASN][1000 genomes]
rs518698	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs520277	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs531658	1.00[EUR][1000 genomes]
rs539008	0.82[ASN][1000 genomes]
rs539250	0.80[ASN][1000 genomes]
rs554812	0.82[ASN][1000 genomes]
rs569741	0.82[ASN][1000 genomes]
rs57371796	1.00[EUR][1000 genomes]
rs575081	0.82[ASN][1000 genomes]
rs58010797	0.80[ASN][1000 genomes]
rs58488481	0.82[ASN][1000 genomes]
rs58721876	1.00[ASN][1000 genomes]
rs59283629	1.00[ASN][1000 genomes]
rs59863478	1.00[EUR][1000 genomes]
rs60421451	0.98[ASN][1000 genomes]
rs60579179	0.80[ASN][1000 genomes]
rs61431997	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs621816	1.00[ASN][1000 genomes]
rs7110262	1.00[ASN][1000 genomes]
rs7121001	0.80[ASN][1000 genomes]
rs73498137	1.00[EUR][1000 genomes]
rs73498145	1.00[EUR][1000 genomes]
rs747621	1.00[EUR][1000 genomes]
rs7950596	1.00[JPT][hapmap]
rs7950922	0.93[ASN][1000 genomes]
rs7951858	0.98[ASN][1000 genomes]
rs7952435	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9666856	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription 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	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
15	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
16	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
17	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
21	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
22	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
23	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
25	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
26	nsv897672	chr11:63979643-64082807	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
27	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
28	nsv897677	chr11:63994692-64023971	Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	85 gene(s)	inside rSNPs	diseases
29	nsv897678	chr11:63994692-64026144	Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	85 gene(s)	inside rSNPs	diseases
30	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
31	nsv541064	chr11:63998625-64036450	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases
32	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
33	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64020000-64023400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:64020000-64023600	Weak transcription	Primary T cells from cord blood	blood
3	chr11:64020000-64027000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:64020000-64036400	Weak transcription	Fetal Kidney	kidney
5	chr11:64020200-64030200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr11:64020200-64034800	Weak transcription	Right Atrium	heart
7	chr11:64020200-64035400	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr11:64020400-64023800	Weak transcription	Aorta	Aorta
9	chr11:64020400-64026000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr11:64020400-64026000	Weak transcription	HepG2	liver
11	chr11:64020400-64027000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr11:64020400-64035200	Weak transcription	Primary B cells from cord blood	blood
13	chr11:64020400-64036000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr11:64020600-64023600	Weak transcription	Fetal Lung	lung
15	chr11:64020600-64023800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr11:64020600-64027200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr11:64020600-64035000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr11:64020600-64035600	Weak transcription	Primary B cells from peripheral blood	blood
19	chr11:64020800-64023000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr11:64020800-64023200	Weak transcription	Colon Smooth Muscle	Colon
21	chr11:64020800-64023600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr11:64020800-64024400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr11:64020800-64029800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:64021000-64023200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:64021000-64023800	Weak transcription	Brain Anterior Caudate	brain
26	chr11:64021000-64024400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr11:64021000-64035600	Weak transcription	Brain Angular Gyrus	brain
28	chr11:64021000-64035600	Weak transcription	Fetal Heart	heart
29	chr11:64021200-64023800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr11:64021200-64024400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr11:64021200-64024600	Strong transcription	H9 Cell Line	embryonic stem cell
32	chr11:64021200-64034800	Strong transcription	Fetal Intestine Small	intestine
33	chr11:64021200-64034800	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:64021200-64035600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr11:64021400-64023200	Weak transcription	NH-A	brain
36	chr11:64021400-64023800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr11:64021400-64023800	Strong transcription	NHEK	skin
38	chr11:64021400-64024000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:64021400-64025200	Weak transcription	Brain Germinal Matrix	brain
40	chr11:64021400-64026800	Weak transcription	GM12878-XiMat	blood
41	chr11:64021400-64030400	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr11:64021400-64035800	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr11:64021600-64023200	Weak transcription	HSMM	muscle
44	chr11:64021600-64023400	Weak transcription	NHDF-Ad	bronchial
45	chr11:64021600-64023800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr11:64021600-64023800	Weak transcription	HSMMtube	muscle
47	chr11:64021600-64023800	Strong transcription	K562	blood
48	chr11:64021600-64024400	Genic enhancers	Hela-S3	cervix
49	chr11:64021600-64025600	Weak transcription	Brain Substantia Nigra	brain
50	chr11:64021600-64029200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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