Variant report

Variant	rs17718535
Chromosome Location	chr5:147452834-147452835
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 110 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10074782	0.84[CHB][hapmap];0.81[EUR][1000 genomes]
rs10491340	1.00[AFR][1000 genomes]
rs10491341	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs10491342	0.81[EUR][1000 genomes]
rs11948836	0.81[EUR][1000 genomes]
rs11950029	0.84[EUR][1000 genomes]
rs11951613	0.84[EUR][1000 genomes]
rs11951614	0.84[EUR][1000 genomes]
rs11952442	0.84[EUR][1000 genomes]
rs11954011	0.84[EUR][1000 genomes]
rs11955612	0.84[EUR][1000 genomes]
rs11956309	0.84[EUR][1000 genomes]
rs11957191	0.84[EUR][1000 genomes]
rs11957744	0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs11958071	0.84[EUR][1000 genomes]
rs11958866	0.84[EUR][1000 genomes]
rs11960620	0.82[CHB][hapmap];0.84[EUR][1000 genomes]
rs12332673	0.81[EUR][1000 genomes]
rs1363718	0.84[EUR][1000 genomes]
rs1363719	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs1363720	0.84[EUR][1000 genomes]
rs1422985	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1422986	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17107575	0.86[CHB][hapmap];0.84[EUR][1000 genomes]
rs17107650	0.84[EUR][1000 genomes]
rs17107665	0.84[EUR][1000 genomes]
rs17107672	0.84[EUR][1000 genomes]
rs17107673	0.84[EUR][1000 genomes]
rs17107676	0.84[EUR][1000 genomes]
rs17107680	0.84[EUR][1000 genomes]
rs17107705	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17599451	1.00[AFR][1000 genomes]
rs17599528	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs17641707	0.86[CHB][hapmap];1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs17718366	0.84[EUR][1000 genomes]
rs17718385	0.84[EUR][1000 genomes]
rs17718403	0.84[EUR][1000 genomes]
rs17718420	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs17718511	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17718737	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17774892	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs17774947	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs17775044	0.84[EUR][1000 genomes]
rs17775080	0.84[EUR][1000 genomes]
rs17775092	0.84[EUR][1000 genomes]
rs17775104	0.84[EUR][1000 genomes]
rs17775739	0.84[CHB][hapmap]
rs17860502	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1833769	0.84[EUR][1000 genomes]
rs2032866	0.84[EUR][1000 genomes]
rs2052530	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs2112768	0.84[EUR][1000 genomes]
rs2112769	0.84[EUR][1000 genomes]
rs2287774	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2303069	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3752677	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3777138	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[EUR][1000 genomes]
rs3815734	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4705050	0.84[EUR][1000 genomes]
rs4705051	0.84[EUR][1000 genomes]
rs4705052	0.84[EUR][1000 genomes]
rs4705053	0.84[EUR][1000 genomes]
rs4705219	0.84[EUR][1000 genomes]
rs4705220	0.84[EUR][1000 genomes]
rs5014785	0.84[EUR][1000 genomes]
rs56714312	0.81[EUR][1000 genomes]
rs56945766	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57608902	0.84[EUR][1000 genomes]
rs58212044	0.84[EUR][1000 genomes]
rs58237290	0.84[EUR][1000 genomes]
rs58359628	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58789871	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs58923221	0.84[EUR][1000 genomes]
rs59133736	0.84[EUR][1000 genomes]
rs59140447	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59581675	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs59900981	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60978485	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61547850	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61612041	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6872206	0.81[EUR][1000 genomes]
rs6873949	0.84[EUR][1000 genomes]
rs6881420	0.84[EUR][1000 genomes]
rs6891750	0.84[EUR][1000 genomes]
rs6892970	0.84[EUR][1000 genomes]
rs6896204	0.84[EUR][1000 genomes]
rs73269110	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73269112	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73269121	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73271110	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73794613	0.81[EUR][1000 genomes]
rs73794614	0.84[EUR][1000 genomes]
rs73794615	0.84[EUR][1000 genomes]
rs73794633	0.84[EUR][1000 genomes]
rs7703112	0.84[EUR][1000 genomes]
rs7705278	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7706528	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7714855	0.84[EUR][1000 genomes]
rs7719473	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7721002	0.84[EUR][1000 genomes]
rs7727019	0.84[EUR][1000 genomes]
rs7733255	0.84[EUR][1000 genomes]
rs953310	0.84[EUR][1000 genomes]
rs984836	0.84[EUR][1000 genomes]
rs9885178	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033838	chr5:147360521-147484014	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv933016	chr5:147395849-147453701	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv933225	chr5:147395849-147486560	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	esv1834529	chr5:147442199-147456843	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island 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	chr5:147437200-147457400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:147437800-147463800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:147443800-147455400	Weak transcription	Esophagus	oesophagus
4	chr5:147449800-147453000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr5:147450000-147453000	Enhancers	NHEK	skin
6	chr5:147450400-147469000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:147450600-147468600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr5:147450800-147474000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr5:147451000-147470000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:147452400-147453200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:147452800-147453600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:147452800-147454200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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