Variant report

Variant	rs34137954
Chromosome Location	chr11:64865006-64865007
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64570549..64572322-chr11:64863262..64865763,3	MCF-7	breast:
2	chr11:64863685..64865502-chr11:64899385..64903204,3	K562	blood:
3	chr11:64862263..64865019-chr11:64949588..64952291,3	MCF-7	breast:
4	chr11:64793758..64795371-chr11:64862909..64865149,3	MCF-7	breast:
5	chr11:64793292..64796781-chr11:64862367..64865846,4	K562	blood:
6	chr11:64569782..64572996-chr11:64862581..64865602,3	K562	blood:
7	chr11:64793819..64796993-chr11:64862794..64865846,5	K562	blood:
8	chr11:64779913..64786139-chr11:64862018..64866625,10	K562	blood:
9	chr11:64764254..64767473-chr11:64863464..64866192,3	K562	blood:
10	chr11:64779401..64787584-chr11:64862745..64867550,9	MCF-7	breast:
11	chr11:64607780..64614825-chr11:64861884..64865172,9	MCF-7	breast:
12	chr11:64806669..64810557-chr11:64862016..64868359,8	K562	blood:
13	chr11:64864336..64865901-chr11:64948929..64951188,2	MCF-7	breast:
14	chr11:64806772..64810496-chr11:64862454..64866792,5	K562	blood:
15	chr11:64806644..64812839-chr11:64862132..64865938,9	MCF-7	breast:
16	chr11:64860579..64868255-chr11:64873377..64881831,25	K562	blood:
17	chr11:64862526..64865749-chr11:64882167..64886670,6	K562	blood:
18	chr11:64805658..64811611-chr11:64862545..64865451,9	MCF-7	breast:
19	chr11:64862784..64865189-chr11:65028595..65030936,2	K562	blood:
20	chr11:64646046..64648742-chr11:64862657..64865181,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254614	Chromatin interaction
ENSG00000168062	Chromatin interaction
ENSG00000270775	Chromatin interaction
ENSG00000110047	Chromatin interaction
ENSG00000110025	Chromatin interaction
ENSG00000149809	Chromatin interaction
ENSG00000273003	Chromatin interaction
ENSG00000014138	Chromatin interaction
ENSG00000171219	Chromatin interaction
ENSG00000014216	Chromatin interaction
ENSG00000254501	Chromatin interaction
ENSG00000174276	Chromatin interaction
ENSG00000213465	Chromatin interaction
ENSG00000255173	Chromatin interaction
ENSG00000168061	Chromatin interaction
ENSG00000149823	Chromatin interaction
ENSG00000168067	Chromatin interaction
ENSG00000162298	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs769439	0.87[MKK][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
2	nsv897709	chr11:64772545-64870779	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv897710	chr11:64772545-64885445	Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS 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 miRNA target site	99 gene(s)	inside rSNPs	diseases
4	nsv897711	chr11:64772545-64900270	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
5	nsv897712	chr11:64856695-64882789	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64863000-64865200	Enhancers	Fetal Heart	heart
2	chr11:64863600-64865200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:64864200-64865200	Enhancers	Spleen	Spleen
4	chr11:64864200-64879400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:64864400-64865200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr11:64864400-64874600	Weak transcription	Aorta	Aorta
7	chr11:64864400-64878000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:64864600-64865200	Enhancers	Primary B cells from cord blood	blood
9	chr11:64864600-64865400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr11:64864600-64865400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:64864600-64865800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:64864600-64866000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
13	chr11:64864600-64866400	Weak transcription	Lung	lung
14	chr11:64864600-64869000	Weak transcription	Left Ventricle	heart
15	chr11:64864600-64873000	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr11:64864600-64874600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:64864600-64876400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr11:64864800-64865200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:64864800-64865200	Genic enhancers	Primary B cells from peripheral blood	blood
20	chr11:64864800-64865200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:64864800-64865200	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr11:64864800-64865200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr11:64864800-64865200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:64864800-64865200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr11:64864800-64865200	Enhancers	Adipose Nuclei	Adipose
26	chr11:64864800-64865200	Enhancers	Brain Angular Gyrus	brain
27	chr11:64864800-64865200	Enhancers	Fetal Intestine Large	intestine
28	chr11:64864800-64865200	Genic enhancers	Fetal Muscle Trunk	muscle
29	chr11:64864800-64865200	Enhancers	GM12878-XiMat	blood
30	chr11:64864800-64865400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr11:64864800-64865400	Genic enhancers	Brain Hippocampus Middle	brain
32	chr11:64864800-64865400	Genic enhancers	Fetal Muscle Leg	muscle
33	chr11:64864800-64865400	Genic enhancers	Fetal Thymus	thymus
34	chr11:64864800-64865600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr11:64864800-64865600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:64864800-64865600	Genic enhancers	Primary T cells fromperipheralblood	blood
37	chr11:64864800-64865600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr11:64864800-64865800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr11:64864800-64865800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr11:64864800-64865800	Enhancers	Liver	Liver
41	chr11:64864800-64866200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr11:64864800-64866200	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr11:64864800-64866400	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr11:64864800-64866400	Weak transcription	Psoas Muscle	Psoas
45	chr11:64864800-64866800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr11:64864800-64866800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:64864800-64867400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr11:64864800-64867800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr11:64864800-64868600	Weak transcription	Osteobl	bone
50	chr11:64864800-64869000	Weak transcription	Pancreas	Pancrea

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