Variant report

Variant	rs11006897
Chromosome Location	chr10:28436534-28436535
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:28433533..28435848-chr10:28435858..28437751,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10740785	0.82[CHB][hapmap]
rs10826407	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10826408	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10826424	0.86[CHB][hapmap]
rs11006896	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11006902	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs11006903	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs11006920	0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12251587	0.82[CHB][hapmap]
rs12251924	1.00[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs12254584	1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs12255686	0.86[CHB][hapmap]
rs12259869	0.95[ASN][1000 genomes]
rs12261363	1.00[CHB][hapmap];0.95[ASN][1000 genomes]
rs12264184	1.00[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs12268470	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12573451	0.84[JPT][hapmap]
rs12766231	1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs1937808	0.82[CHB][hapmap]
rs2763321	0.95[CHB][hapmap];0.85[JPT][hapmap];0.93[ASN][1000 genomes]
rs2985523	0.81[JPT][hapmap]
rs2997202	0.88[ASN][1000 genomes]
rs3901407	0.83[CHB][hapmap]
rs3905706	0.83[CHB][hapmap]
rs4408232	0.92[ASN][1000 genomes]
rs4568902	0.82[CHB][hapmap]
rs4747615	0.94[ASN][1000 genomes]
rs4747616	0.82[CEU][hapmap]
rs4749310	0.95[CHB][hapmap];0.80[JPT][hapmap];0.93[ASN][1000 genomes]
rs4749311	1.00[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.81[YRI][hapmap];0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4749313	0.95[ASN][1000 genomes]
rs58368296	0.99[ASN][1000 genomes]
rs7068687	0.83[CHB][hapmap]
rs7081378	1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs7085245	1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs7088552	0.82[CHB][hapmap]
rs7097357	0.93[ASN][1000 genomes]
rs7101051	1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs7922685	0.82[CHB][hapmap]
rs9663596	0.95[CHB][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS 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 miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1042524	chr10:28290149-28506812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv831816	chr10:28304698-28493635	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv525448	chr10:28337570-28563732	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv831817	chr10:28369836-28539930	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv1848511	chr10:28373644-28464753	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv894989	chr10:28384098-28449974	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv949151	chr10:28386125-28455221	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
10	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
11	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28376000-28438400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr10:28403600-28443200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr10:28413200-28440600	Weak transcription	Left Ventricle	heart
4	chr10:28417000-28449200	Weak transcription	Pancreas	Pancrea
5	chr10:28417600-28458000	Weak transcription	Aorta	Aorta
6	chr10:28426800-28438400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr10:28427200-28438200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr10:28427200-28440600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr10:28427200-28448600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr10:28430000-28437600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr10:28430600-28441400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr10:28431600-28436600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr10:28432000-28439600	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr10:28434200-28439000	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr10:28434400-28437600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr10:28434400-28439200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr10:28434800-28440400	Weak transcription	Primary B cells from cord blood	blood
18	chr10:28434800-28446200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr10:28435200-28437600	Weak transcription	Fetal Intestine Large	intestine
20	chr10:28435200-28441800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr10:28435400-28438000	Weak transcription	HepG2	liver
22	chr10:28435600-28436800	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr10:28435600-28437200	Strong transcription	Primary T cells from cord blood	blood
24	chr10:28435600-28438800	Weak transcription	Esophagus	oesophagus
25	chr10:28435600-28439000	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr10:28435800-28436600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:28435800-28437000	Strong transcription	Primary neutrophils fromperipheralblood	blood
28	chr10:28435800-28437200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr10:28436000-28436800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr10:28436000-28439000	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr10:28436200-28436800	Enhancers	Fetal Lung	lung
32	chr10:28436200-28437200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr10:28436400-28436800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr10:28436400-28436800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:28436400-28436800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr10:28436400-28437000	Enhancers	H9 Cell Line	embryonic stem cell
37	chr10:28436400-28437000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr10:28436400-28437000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr10:28436400-28437200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr10:28436400-28437200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr10:28436400-28437200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr10:28436400-28437200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr10:28436400-28437200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr10:28436400-28437400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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