Variant report

Variant	rs4074836
Chromosome Location	chr9:95712149-95712150
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:95706512..95708726-chr9:95712017..95714192,2	K562	blood:
2	chr9:95711746..95713546-chr9:95716318..95718556,2	MCF-7	breast:
3	chr9:95706988..95710231-chr9:95710858..95713457,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000127084	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs12003440	0.91[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs12003885	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13284600	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13293147	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13294147	0.94[ASN][1000 genomes]
rs17886128	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34405247	0.90[ASN][1000 genomes]
rs34739544	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34953814	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35449185	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35721889	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4078292	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4260949	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4744160	0.88[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs58264693	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7024752	0.94[ASN][1000 genomes]
rs7035881	0.92[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7043469	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7856681	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7858810	0.82[AMR][1000 genomes]
rs7859461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7873125	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9942865	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831654	chr9:95542920-95720961	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv526296	chr9:95708192-96030392	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95709000-95712200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
2	chr9:95710000-95712200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
3	chr9:95710000-95713000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:95710200-95712400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr9:95710200-95715800	Weak transcription	Spleen	Spleen
6	chr9:95710200-95716400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:95710400-95712200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
8	chr9:95710600-95712400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
9	chr9:95710600-95712400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr9:95710600-95713200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr9:95710800-95712200	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr9:95711000-95712400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr9:95711000-95712400	Flanking Active TSS	Brain Germinal Matrix	brain
14	chr9:95711000-95714800	Weak transcription	Fetal Lung	lung
15	chr9:95711000-95715400	Enhancers	Fetal Brain Male	brain
16	chr9:95711200-95712200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:95711400-95712200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:95711400-95714800	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr9:95711400-95715800	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr9:95711600-95713400	Enhancers	Esophagus	oesophagus
21	chr9:95711600-95715000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr9:95711800-95712200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
23	chr9:95711800-95712200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr9:95712000-95712200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr9:95712000-95712200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:95712000-95712200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:95712000-95712200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr9:95712000-95712200	Flanking Active TSS	Fetal Brain Female	brain
29	chr9:95712000-95712600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr9:95712000-95713400	Enhancers	NHEK	skin
31	chr9:95712000-95714000	Enhancers	Primary T cells from cord blood	blood
32	chr9:95712000-95714800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:95712000-95715400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr9:95712000-95715800	Weak transcription	Lung	lung
35	chr9:95712000-95717200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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