Variant report

Variant	rs7673304
Chromosome Location	chr4:165897834-165897835
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:165896605..165899172-chr4:165907116..165908745,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000248229	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17046014	1.00[MEX][hapmap]
rs7680096	1.00[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019150	chr4:165505585-165907924	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv1026152	chr4:165622244-166027447	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv537336	chr4:165622244-166027447	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Active 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	36 gene(s)	inside rSNPs	diseases
4	nsv1022210	chr4:165792630-166251612	Genic enhancers Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv537337	chr4:165792630-166251612	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv880382	chr4:165793001-165964290	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	esv2757965	chr4:165801816-165976350	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	esv2759299	chr4:165801816-165976350	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	nsv528686	chr4:165814359-165930168	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
10	nsv1015970	chr4:165852926-165973078	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv1021905	chr4:165852926-166212878	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
12	nsv830140	chr4:165855999-165956612	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv533191	chr4:165879671-166171638	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165878800-165898200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:165879400-165898000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr4:165879800-165898000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr4:165881600-165898000	Weak transcription	Osteobl	bone
5	chr4:165884600-165898200	Weak transcription	Ovary	ovary
6	chr4:165887000-165898200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr4:165887200-165898000	Weak transcription	Primary B cells from cord blood	blood
8	chr4:165888800-165898000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:165892200-165898200	Weak transcription	Lung	lung
10	chr4:165894000-165898000	Weak transcription	Fetal Brain Female	brain
11	chr4:165894400-165898400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr4:165894800-165898000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr4:165895000-165898200	Weak transcription	Brain Germinal Matrix	brain
14	chr4:165895600-165898000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr4:165896000-165898200	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr4:165896200-165898000	Weak transcription	Colon Smooth Muscle	Colon
17	chr4:165896400-165898200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:165897600-165898000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr4:165897600-165898000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:165897600-165898000	Enhancers	Fetal Heart	heart
21	chr4:165897600-165898000	Enhancers	Fetal Intestine Large	intestine
22	chr4:165897600-165898000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr4:165897600-165898000	Enhancers	Fetal Lung	lung
24	chr4:165897600-165898000	Enhancers	NHLF	lung
25	chr4:165897600-165898200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:165897600-165898200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr4:165897600-165899000	Active TSS	GM12878-XiMat	blood
28	chr4:165897600-165899400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:165897600-165899400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr4:165897800-165898000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:165897800-165898000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:165897800-165898000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:165897800-165898000	Enhancers	Adipose Nuclei	Adipose
34	chr4:165897800-165898000	Flanking Active TSS	Fetal Intestine Small	intestine
35	chr4:165897800-165898000	Genic enhancers	Fetal Muscle Leg	muscle
36	chr4:165897800-165898000	Enhancers	Fetal Thymus	thymus
37	chr4:165897800-165898000	Enhancers	Left Ventricle	heart
38	chr4:165897800-165898200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:165897800-165898200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr4:165897800-165898200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr4:165897800-165898200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:165897800-165898200	Enhancers	Primary B cells from peripheral blood	blood
43	chr4:165897800-165898200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr4:165897800-165898200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:165897800-165898200	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr4:165897800-165898200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
47	chr4:165897800-165898200	Flanking Active TSS	NHDF-Ad	bronchial
48	chr4:165897800-165898400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:165897800-165898600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:165897800-165898800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links