Variant report

Variant	rs10836351
Chromosome Location	chr11:35259788-35259789
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35256103..35261501-chr11:35384186..35388588,8	MCF-7	breast:
2	chr11:35249750..35251832-chr11:35258171..35261119,2	K562	blood:
3	chr11:35258928..35261277-chr11:35264057..35266573,2	K562	blood:
4	chr11:35258018..35260931-chr11:35412299..35415204,2	MCF-7	breast:
5	chr11:34961886..34962391-chr11:35259545..35260066,2	MCF-7	breast:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1043101	0.81[JPT][hapmap]
rs10488812	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10768116	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10768122	0.81[JPT][hapmap]
rs10836356	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11033036	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17449131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3088168	0.81[JPT][hapmap]
rs4755392	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7104704	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7115638	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs932633	0.90[ASN][1000 genomes]
rs932635	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv541003	chr11:35122694-35261451	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription 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 miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv541004	chr11:35122694-35297414	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv897218	chr11:35241989-35261374	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv897220	chr11:35242907-35261374	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv897221	chr11:35242907-35265444	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
7	nsv897222	chr11:35244044-35261374	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35247000-35263200	Weak transcription	HSMMtube	muscle
2	chr11:35251400-35259800	Weak transcription	Gastric	stomach
3	chr11:35253000-35260400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:35254600-35264000	Weak transcription	Colon Smooth Muscle	Colon
5	chr11:35254600-35264000	Weak transcription	NHLF	lung
6	chr11:35255400-35266800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr11:35255600-35260800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:35256600-35259800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr11:35256600-35260000	Enhancers	NHEK	skin
10	chr11:35256600-35260200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr11:35256600-35260200	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr11:35256600-35260200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr11:35256600-35260400	Enhancers	Primary T cells from cord blood	blood
14	chr11:35256600-35260400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr11:35256600-35261200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr11:35256800-35260000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr11:35256800-35260600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:35257000-35260000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr11:35257400-35260200	Enhancers	Fetal Thymus	thymus
20	chr11:35257400-35261800	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr11:35257600-35260200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr11:35258000-35259800	Enhancers	Placenta	Placenta
23	chr11:35258200-35263000	Weak transcription	HSMM	muscle
24	chr11:35258400-35260800	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr11:35258400-35261200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr11:35258400-35263400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:35258400-35264000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:35258400-35267400	Weak transcription	Aorta	Aorta
29	chr11:35258400-35269000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:35258600-35259800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr11:35258600-35260200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:35258600-35260400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:35258600-35260400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:35258600-35260800	Enhancers	Fetal Lung	lung
35	chr11:35258600-35261400	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr11:35258600-35263000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr11:35258600-35263200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:35258800-35260200	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr11:35258800-35264000	Weak transcription	NHDF-Ad	bronchial
40	chr11:35258800-35267400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr11:35259000-35259800	Enhancers	Thymus	Thymus
42	chr11:35259000-35260200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr11:35259000-35263400	Weak transcription	Osteobl	bone
44	chr11:35259200-35259800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr11:35259200-35260000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr11:35259200-35260000	Enhancers	GM12878-XiMat	blood
47	chr11:35259200-35260200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr11:35259200-35270200	Weak transcription	Stomach Mucosa	stomach
49	chr11:35259400-35259800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr11:35259400-35259800	Enhancers	H1 Cell Line	embryonic stem cell

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