Variant report

Variant	rs17515832
Chromosome Location	chr4:119142002-119142003
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10001926	0.87[ASN][1000 genomes]
rs10002634	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10008013	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10014055	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10014957	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10016206	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10016301	0.97[ASN][1000 genomes]
rs10018844	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10024837	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10025690	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10033927	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10213280	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1028091	1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[ASN][1000 genomes]
rs1045817	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11721634	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11723877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11723996	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11726746	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11726838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11727684	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11727817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11728941	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11730327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11730687	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11731179	0.93[ASN][1000 genomes]
rs11734145	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11930782	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11933280	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11934183	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11944227	1.00[ASN][1000 genomes]
rs11945329	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11945537	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11945882	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11947244	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11947630	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13114867	0.97[ASN][1000 genomes]
rs13129847	0.97[ASN][1000 genomes]
rs13435006	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403845	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403846	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1523744	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1523745	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1523746	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1589718	0.97[ASN][1000 genomes]
rs17516430	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs17516450	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs17516575	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs17594054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17594243	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1996725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030633	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2030634	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2204269	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2271577	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2271578	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2272160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2292598	1.00[YRI][hapmap]
rs28396217	1.00[ASN][1000 genomes]
rs28508556	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28661939	1.00[CEU][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3805195	0.81[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs3817274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4546315	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56007507	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56258393	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56305917	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56339949	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56390335	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57605165	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58798110	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60858456	0.93[ASN][1000 genomes]
rs61342457	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61443542	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62326151	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6534088	0.93[ASN][1000 genomes]
rs6822408	0.93[ASN][1000 genomes]
rs6822996	1.00[ASN][1000 genomes]
rs6842372	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6842689	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6853304	0.81[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap]
rs6853879	0.97[ASN][1000 genomes]
rs6855052	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6855536	0.90[ASN][1000 genomes]
rs6856076	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71608347	0.97[ASN][1000 genomes]
rs71608349	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72907147	0.93[ASN][1000 genomes]
rs72907175	0.93[ASN][1000 genomes]
rs72909175	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72909186	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72917104	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72917146	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72917175	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72917179	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7661522	0.97[ASN][1000 genomes]
rs7685455	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9992827	0.97[ASN][1000 genomes]
rs9996753	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9996762	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1009076	chr4:118949490-119269424	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1001236	chr4:118949490-119271243	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv1008236	chr4:118989467-119154024	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv34038	chr4:119035124-119455391	Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv1001138	chr4:119095147-119461837	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv537230	chr4:119095147-119461837	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv4485	chr4:119103349-119144334	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
9	nsv1002771	chr4:119125361-119571237	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	nsv1003731	chr4:119138262-119506032	Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17515832	SNHG8	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119137200-119142200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:119140000-119145600	Enhancers	Dnd41	blood
3	chr4:119141800-119142200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr4:119142000-119144000	Enhancers	Primary T cells from cord blood	blood

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