Variant report

Variant	rs35700033
Chromosome Location	chr5:179670116-179670117
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:179669950..179671788-chr5:179672215..179674940,2	MCF-7	breast:
2	chr5:179669999..179672400-chr5:179718996..179720849,2	K562	blood:

Variant related genes	Relation type
ENSG00000050748	Chromatin interaction
ENSG00000248367	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17627580	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17627695	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17684072	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34313563	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34430669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34517134	1.00[AMR][1000 genomes]
rs34520158	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34755646	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34862489	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34868204	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35827396	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36048247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6891707	1.00[EUR][1000 genomes]
rs73811335	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948909	chr5:179249099-179772640	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv1033706	chr5:179402769-179806356	Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	esv2758032	chr5:179534477-179729944	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv2759398	chr5:179534477-179729944	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv1023914	chr5:179649883-180040672	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv537983	chr5:179649883-180040672	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179651600-179678000	Weak transcription	Fetal Heart	heart
2	chr5:179653600-179714600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:179655000-179679600	Weak transcription	Stomach Mucosa	stomach
4	chr5:179655400-179712600	ZNF genes & repeats	Liver	Liver
5	chr5:179655800-179675400	Strong transcription	Primary B cells from cord blood	blood
6	chr5:179656200-179675000	Strong transcription	Skeletal Muscle Female	skeletal muscle
7	chr5:179656600-179703000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
8	chr5:179657400-179673600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:179657400-179674400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:179657800-179674400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:179657800-179697000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:179658400-179670600	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr5:179658400-179670800	Strong transcription	Fetal Muscle Leg	muscle
14	chr5:179658400-179672600	Strong transcription	Thymus	Thymus
15	chr5:179658400-179679200	Strong transcription	Primary T cells from cord blood	blood
16	chr5:179658800-179680400	Weak transcription	Fetal Kidney	kidney
17	chr5:179659000-179670800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr5:179659000-179677600	Strong transcription	Dnd41	blood
19	chr5:179659200-179672600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr5:179659200-179674200	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr5:179659400-179674800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:179659600-179674200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr5:179660000-179670800	Strong transcription	Primary B cells from peripheral blood	blood
24	chr5:179660200-179671200	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr5:179660200-179671400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr5:179660200-179672800	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:179660200-179679800	Weak transcription	HUVEC	blood vessel
28	chr5:179660400-179677600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr5:179660600-179670600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:179660600-179670800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr5:179660600-179671800	Weak transcription	HMEC	breast
32	chr5:179660800-179670200	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr5:179660800-179671800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:179660800-179672000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:179660800-179706800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:179661000-179674200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:179661400-179674200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr5:179661800-179673800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr5:179662000-179670800	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr5:179662400-179670200	Strong transcription	Stomach Smooth Muscle	stomach
41	chr5:179662600-179670600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:179663000-179670600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr5:179663000-179670600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr5:179663200-179670600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr5:179663200-179670800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr5:179663200-179671000	Strong transcription	Fetal Intestine Large	intestine
47	chr5:179663400-179672200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:179664400-179677000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr5:179665800-179670600	Strong transcription	Brain Hippocampus Middle	brain
50	chr5:179665800-179670600	Strong transcription	Right Ventricle	heart

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