Variant report

Variant	rs566264770
Chromosome Location	chr11:63755950-63755951
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:63752288..63756029-chr11:63763681..63768717,11	MCF-7	breast:
2	chr11:63739151..63744415-chr11:63752010..63756596,9	MCF-7	breast:
3	chr1:149857624..149859749-chr11:63753842..63756794,2	MCF-7	breast:
4	chr11:63684119..63685906-chr11:63753939..63756013,2	MCF-7	breast:
5	chr11:63754724..63756802-chr11:63908470..63911045,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167770	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000167771	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051171	chr11:62987064-63835715	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription 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 target site	100 gene(s)	inside rSNPs	diseases
2	nsv468590	chr11:63639881-63783352	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv555181	chr11:63639881-63783352	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	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
7	nsv897639	chr11:63691049-63844683	Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
8	esv1849906	chr11:63719273-63880383	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv1042075	chr11:63732454-63813164	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	esv29993	chr11:63738642-63864211	Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription 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 miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv897640	chr11:63744152-63835611	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv897641	chr11:63744152-63844683	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
13	nsv897642	chr11:63744152-63866959	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
14	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
15	nsv897643	chr11:63754986-63844683	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
16	nsv897644	chr11:63754986-63849330	Bivalent Enhancer Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
17	nsv897645	chr11:63754986-63859751	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
18	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

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63754600-63758600	Weak transcription	Aorta	Aorta
2	chr11:63754800-63756000	Enhancers	Fetal Heart	heart
3	chr11:63754800-63756400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:63754800-63757600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:63754800-63767600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:63755000-63756000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:63755000-63756000	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:63755000-63756000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr11:63755000-63756000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:63755000-63756000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr11:63755000-63756000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr11:63755000-63756200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
13	chr11:63755000-63756200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr11:63755000-63756200	Genic enhancers	Fetal Muscle Trunk	muscle
15	chr11:63755000-63766600	Weak transcription	Right Atrium	heart
16	chr11:63755000-63769000	Weak transcription	Fetal Kidney	kidney
17	chr11:63755200-63756000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:63755200-63756000	Transcr. at gene 5' and 3'	Dnd41	blood
19	chr11:63755200-63756200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:63755200-63756400	Genic enhancers	Esophagus	oesophagus
21	chr11:63755200-63756400	Genic enhancers	K562	blood
22	chr11:63755200-63757600	Weak transcription	Left Ventricle	heart
23	chr11:63755200-63757600	Weak transcription	HSMMtube	muscle
24	chr11:63755200-63757800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr11:63755200-63761200	Weak transcription	HUVEC	blood vessel
26	chr11:63755200-63762000	Weak transcription	Small Intestine	intestine
27	chr11:63755200-63766600	Weak transcription	Stomach Mucosa	stomach
28	chr11:63755200-63775200	Weak transcription	Psoas Muscle	Psoas
29	chr11:63755400-63756000	Genic enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:63755400-63756000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr11:63755400-63756000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr11:63755400-63756000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr11:63755400-63756000	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr11:63755400-63756000	Weak transcription	Liver	Liver
35	chr11:63755400-63756000	Genic enhancers	Fetal Intestine Large	intestine
36	chr11:63755400-63756000	Genic enhancers	Fetal Intestine Small	intestine
37	chr11:63755400-63756000	Genic enhancers	Stomach Smooth Muscle	stomach
38	chr11:63755400-63756000	Genic enhancers	A549	lung
39	chr11:63755400-63756000	Genic enhancers	Hela-S3	cervix
40	chr11:63755400-63756200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr11:63755400-63756200	Weak transcription	Primary T cells from cord blood	blood
42	chr11:63755400-63756200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:63755400-63756400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr11:63755400-63756400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr11:63755400-63756600	Strong transcription	Brain Germinal Matrix	brain
46	chr11:63755400-63756600	Strong transcription	Osteobl	bone
47	chr11:63755400-63756800	Weak transcription	Fetal Lung	lung
48	chr11:63755400-63757400	Weak transcription	Gastric	stomach
49	chr11:63755400-63757600	Weak transcription	Brain Cingulate Gyrus	brain
50	chr11:63755400-63757600	Weak transcription	Colon Smooth Muscle	Colon

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