Variant report

Variant	rs1491369
Chromosome Location	chr4:20917854-20917855
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10428482	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10461094	0.83[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs11727035	0.82[ASN][1000 genomes]
rs13129855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13151383	0.83[ASN][1000 genomes]
rs1347385	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs1352796	0.87[JPT][hapmap]
rs1388326	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs1434948	0.88[ASN][1000 genomes]
rs1434950	0.91[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs1434951	0.97[ASN][1000 genomes]
rs1434952	0.81[ASN][1000 genomes]
rs1434953	0.87[ASN][1000 genomes]
rs1491356	0.87[JPT][hapmap]
rs1491357	0.87[JPT][hapmap]
rs1491361	0.88[JPT][hapmap]
rs1565534	0.87[JPT][hapmap]
rs1836520	0.83[ASN][1000 genomes]
rs4395501	0.91[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs4441750	0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs6447998	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs6447999	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs6811024	0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs6830607	0.80[EUR][1000 genomes]
rs6832672	0.92[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs6833232	0.98[ASN][1000 genomes]
rs6843757	0.91[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap]
rs6858759	0.87[JPT][hapmap]
rs7677635	0.91[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs7677781	0.87[JPT][hapmap]
rs7690016	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs7698780	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010145	chr4:20601908-21057992	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv537052	chr4:20601908-21057992	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv869522	chr4:20724433-20938248	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
7	nsv829877	chr4:20847465-20992544	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv1803304	chr4:20853243-20934396	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv1808703	chr4:20853243-20934396	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv878743	chr4:20888436-20926819	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv878744	chr4:20896318-20951955	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20916200-20918200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
2	chr4:20916200-20918400	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr4:20916400-20918400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr4:20916600-20927800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr4:20916800-20918400	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr4:20917600-20918200	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr4:20917800-20918400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr4:20917800-20920400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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