Variant report

Variant	rs295965
Chromosome Location	chr5:58906099-58906100
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10805516	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs159194	0.85[ASN][1000 genomes]
rs159196	0.89[ASN][1000 genomes]
rs159197	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs177078	0.91[ASN][1000 genomes]
rs186078	0.84[ASN][1000 genomes]
rs190936	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs294477	0.84[ASN][1000 genomes]
rs294478	0.85[ASN][1000 genomes]
rs294479	0.85[ASN][1000 genomes]
rs294481	0.85[ASN][1000 genomes]
rs294482	0.84[ASN][1000 genomes]
rs294483	0.85[ASN][1000 genomes]
rs294484	0.85[ASN][1000 genomes]
rs294485	0.83[ASN][1000 genomes]
rs294486	0.85[ASN][1000 genomes]
rs294492	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs294495	0.92[ASN][1000 genomes]
rs294496	0.92[ASN][1000 genomes]
rs294497	0.92[ASN][1000 genomes]
rs294498	0.89[ASN][1000 genomes]
rs294499	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs294500	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs294501	0.89[ASN][1000 genomes]
rs294502	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs295943	0.93[EUR][1000 genomes]
rs295944	0.89[AFR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs295948	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs295950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295953	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295954	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295955	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295956	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295957	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs295958	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs295960	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs295962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295963	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295964	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295966	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295969	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295971	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295972	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295973	0.99[ASN][1000 genomes]
rs295974	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295975	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs295978	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs295979	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs295980	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs298014	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs298016	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs298017	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs298032	0.83[ASN][1000 genomes]
rs298033	0.83[ASN][1000 genomes]
rs298034	0.88[ASN][1000 genomes]
rs298036	0.91[ASN][1000 genomes]
rs298038	0.89[ASN][1000 genomes]
rs298039	0.89[ASN][1000 genomes]
rs298040	0.92[ASN][1000 genomes]
rs298041	0.93[ASN][1000 genomes]
rs298043	0.92[ASN][1000 genomes]
rs298044	0.93[ASN][1000 genomes]
rs298045	0.93[ASN][1000 genomes]
rs298046	0.92[ASN][1000 genomes]
rs298047	0.93[ASN][1000 genomes]
rs298048	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs298051	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs298052	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs298053	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37569	0.84[ASN][1000 genomes]
rs37570	0.85[ASN][1000 genomes]
rs37571	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv598254	chr5:58715782-58923601	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1031631	chr5:58783629-59015470	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv881708	chr5:58869051-59093198	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1018015	chr5:58889470-59532667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv537766	chr5:58889470-59532667	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv598256	chr5:58893286-58939840	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv598257	chr5:58905769-58946639	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58894800-58910800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:58894800-58910800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:58895800-58911200	Weak transcription	Hela-S3	cervix
4	chr5:58897600-58915800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:58903600-58910000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:58903800-58911200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:58903800-58911400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr5:58903800-58913400	Weak transcription	Colon Smooth Muscle	Colon
9	chr5:58904000-58908000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr5:58904400-58906200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:58904600-58906200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:58904800-58910400	Weak transcription	A549	lung
13	chr5:58905000-58909800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr5:58905200-58910600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr5:58905200-58913200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr5:58905600-58915800	Weak transcription	HSMMtube	muscle
17	chr5:58905800-58906600	Enhancers	Stomach Mucosa	stomach
18	chr5:58905800-58906800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr5:58906000-58907600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr5:58906000-58908800	Weak transcription	Psoas Muscle	Psoas
21	chr5:58906000-58910400	Weak transcription	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links