Variant report

Variant	rs11005399
Chromosome Location	chr10:52134394-52134395
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:52127857..52130924-chr10:52133934..52136011,3	K562	blood:
2	chr10:52127640..52130879-chr10:52134264..52136292,3	K562	blood:
3	chr10:52128591..52131322-chr10:52132559..52135165,2	MCF-7	breast:
4	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
5	chr10:52132819..52134741-chr10:52135257..52137397,2	K562	blood:

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10458673	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10508927	0.89[CEU][hapmap];0.88[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10508928	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10508929	0.88[JPT][hapmap]
rs10733968	0.98[ASN][1000 genomes]
rs10763365	0.82[EUR][1000 genomes]
rs10763373	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10763382	0.89[CEU][hapmap];0.88[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10763392	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10763426	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10763500	0.82[JPT][hapmap]
rs10825789	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10825825	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10825837	0.87[YRI][hapmap]
rs10825861	0.84[CEU][hapmap];0.88[JPT][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10825882	0.89[CEU][hapmap];0.88[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10825904	0.90[CEU][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10825934	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10825978	0.89[CEU][hapmap];0.88[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10825995	0.83[JPT][hapmap]
rs10825996	0.83[JPT][hapmap]
rs10826013	0.88[JPT][hapmap]
rs10826034	0.81[ASN][1000 genomes]
rs11005356	0.90[CEU][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11005415	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11005418	0.85[CEU][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11005454	0.87[YRI][hapmap]
rs11005579	0.81[CEU][hapmap];0.87[JPT][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11005614	0.89[CEU][hapmap];0.88[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11005621	0.84[CEU][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12217648	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1884572	0.90[CEU][hapmap]
rs1916572	0.90[CEU][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2273402	0.82[JPT][hapmap]
rs2339400	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2339401	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2339507	0.82[JPT][hapmap]
rs34122137	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3739989	0.89[CEU][hapmap];0.88[JPT][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4935711	0.82[JPT][hapmap]
rs7074024	0.99[ASN][1000 genomes]
rs7086029	0.89[CEU][hapmap];0.82[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7092749	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7093878	0.99[ASN][1000 genomes]
rs7094029	0.99[ASN][1000 genomes]
rs768185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7896315	0.82[JPT][hapmap]
rs7904375	0.83[EUR][1000 genomes]
rs7920818	0.89[CEU][hapmap];0.82[JPT][hapmap]
rs7922802	1.00[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs910817	0.82[JPT][hapmap]
rs927047	0.82[JPT][hapmap]
rs927048	0.89[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518071	chr10:51595893-52157935	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1054775	chr10:51595893-52392361	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1053903	chr10:51886486-52163991	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1040661	chr10:51886486-52164585	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1051028	chr10:51886486-52164585	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1037118	chr10:51886486-52167442	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv1051087	chr10:51886486-52447295	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv916214	chr10:51886486-52458983	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers 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
9	nsv918212	chr10:51886486-52465482	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
10	nsv817412	chr10:51911034-52432990	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS 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	31 gene(s)	inside rSNPs	diseases
11	esv2830205	chr10:51978430-52135215	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
12	nsv1046850	chr10:52009869-52135542	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv540625	chr10:52009869-52135542	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
14	nsv521273	chr10:52051645-52197847	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
15	nsv430231	chr10:52119046-52163531	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
16	nsv948006	chr10:52127164-52177684	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52104000-52141400	Weak transcription	Pancreas	Pancrea
2	chr10:52104200-52157000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr10:52109400-52134400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:52115800-52142200	Weak transcription	Fetal Intestine Small	intestine
5	chr10:52119400-52136000	Weak transcription	Fetal Brain Male	brain
6	chr10:52120600-52141400	Weak transcription	HSMM	muscle
7	chr10:52121200-52134400	Weak transcription	Fetal Stomach	stomach
8	chr10:52121200-52136600	Weak transcription	Fetal Muscle Trunk	muscle
9	chr10:52121200-52141600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:52121400-52139400	Weak transcription	Placenta	Placenta
11	chr10:52121800-52134400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr10:52121800-52135000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr10:52122800-52134600	Weak transcription	HUVEC	blood vessel
14	chr10:52123400-52134400	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr10:52123400-52134400	Weak transcription	Primary T cells from cord blood	blood
16	chr10:52123400-52134400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr10:52123400-52134400	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr10:52123400-52134800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr10:52123400-52136800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr10:52124600-52139400	Weak transcription	Primary B cells from cord blood	blood
21	chr10:52125400-52134400	Weak transcription	Primary B cells from peripheral blood	blood
22	chr10:52129000-52141600	Weak transcription	Hela-S3	cervix
23	chr10:52129200-52134400	Weak transcription	HMEC	breast
24	chr10:52132400-52135200	Enhancers	Brain Hippocampus Middle	brain
25	chr10:52132800-52134600	Enhancers	Fetal Heart	heart
26	chr10:52132800-52135000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:52132800-52135200	Enhancers	Brain Cingulate Gyrus	brain
28	chr10:52132800-52135400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr10:52132800-52135400	Enhancers	Brain Substantia Nigra	brain
30	chr10:52132800-52135600	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr10:52132800-52135600	Genic enhancers	K562	blood
32	chr10:52133000-52134800	Enhancers	Brain Angular Gyrus	brain
33	chr10:52133000-52134800	Enhancers	Fetal Lung	lung
34	chr10:52133000-52134800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr10:52133000-52134800	Enhancers	Stomach Smooth Muscle	stomach
36	chr10:52133000-52134800	Enhancers	HSMMtube	muscle
37	chr10:52133000-52135400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:52133000-52135400	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr10:52133000-52135400	Enhancers	NHDF-Ad	bronchial
40	chr10:52133000-52135600	Enhancers	Fetal Kidney	kidney
41	chr10:52133000-52136200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr10:52133200-52134400	Weak transcription	NHEK	skin
43	chr10:52133200-52135400	Enhancers	Colon Smooth Muscle	Colon
44	chr10:52133200-52142400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr10:52133400-52135000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:52133400-52135200	Enhancers	Adipose Nuclei	Adipose
47	chr10:52133400-52135400	Enhancers	Rectal Smooth Muscle	rectum
48	chr10:52133600-52134600	Enhancers	NHLF	lung
49	chr10:52133600-52134600	Enhancers	Osteobl	bone
50	chr10:52133600-52134800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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