Variant report

Variant	rs361161
Chromosome Location	chr4:152802623-152802624
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs13113197	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1631928	1.00[CEU][hapmap]
rs165575	0.85[EUR][1000 genomes]
rs165582	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1682083	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs184867	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2113977	0.87[EUR][1000 genomes]
rs244282	0.92[ASN][1000 genomes]
rs244403	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs360919	0.85[EUR][1000 genomes]
rs360920	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs360921	0.92[ASN][1000 genomes]
rs360938	1.00[CEU][hapmap]
rs361110	0.85[EUR][1000 genomes]
rs361132	0.88[ASN][1000 genomes]
rs361133	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs361134	0.97[ASN][1000 genomes]
rs361135	0.97[ASN][1000 genomes]
rs361137	0.97[ASN][1000 genomes]
rs361138	0.97[ASN][1000 genomes]
rs361139	0.97[ASN][1000 genomes]
rs361140	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs361159	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs361160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs361162	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs361164	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs361165	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs361167	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4391010	0.97[ASN][1000 genomes]
rs471230	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs482406	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs486861	0.92[ASN][1000 genomes]
rs497981	0.92[ASN][1000 genomes]
rs509848	1.00[CEU][hapmap]
rs518055	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs523646	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs551375	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs566091	1.00[CEU][hapmap]
rs577900	0.97[ASN][1000 genomes]
rs6815631	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6829557	0.92[ASN][1000 genomes]
rs692907	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432644	chr4:152635395-153023402	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	esv2757086	chr4:152776271-152809738	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759289	chr4:152776271-152809738	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2752342	chr4:152789393-152805443	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2753274	chr4:152789393-152805609	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv595731	chr4:152790580-152831309	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv2754023	chr4:152791533-152805609	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv432650	chr4:152791533-152805609	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv432652	chr4:152791533-152818018	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1030328	chr4:152791533-152875666	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
11	nsv1028836	chr4:152791680-152879097	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	esv3386979	chr4:152802239-152804368	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152796400-152808200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:152796600-152806800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr4:152796600-152807200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr4:152799800-152803000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr4:152801600-152802800	Enhancers	GM12878-XiMat	blood
6	chr4:152801800-152806600	Weak transcription	Fetal Brain Male	brain
7	chr4:152801800-152806800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr4:152801800-152807000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr4:152802200-152807000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:152802400-152806000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:152802600-152803200	Enhancers	Primary T cells fromperipheralblood	blood
12	chr4:152802600-152804200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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