Variant report

Variant	rs10488912
Chromosome Location	chr4:95833910-95833911
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:95783841..95786067-chr4:95832371..95835090,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11097447	0.85[CEU][hapmap]
rs11939949	0.85[CEU][hapmap]
rs11944292	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12508959	0.81[EUR][1000 genomes]
rs12510047	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12511896	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs12511962	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs12512031	0.81[EUR][1000 genomes]
rs12512679	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs12512684	0.81[EUR][1000 genomes]
rs12512864	0.81[EUR][1000 genomes]
rs1348606	0.85[CEU][hapmap]
rs17401285	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs17428494	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs17428501	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs17428550	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs17428564	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs17428585	0.93[CEU][hapmap];0.81[EUR][1000 genomes]
rs17428830	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17429175	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17500351	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs17500448	0.81[EUR][1000 genomes]
rs17500892	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17500926	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17501107	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2023836	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28604506	0.81[EUR][1000 genomes]
rs2865409	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2865411	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs4446318	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4623010	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58645352	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6835267	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7698964	0.86[CEU][hapmap]
rs7699554	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs916875	1.00[CEU][hapmap];0.83[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	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1005816	chr4:95573444-95902704	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv492312	chr4:95823124-96128327	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95816800-95845800	Weak transcription	A549	lung
2	chr4:95831000-95837600	Weak transcription	Fetal Kidney	kidney
3	chr4:95831000-95855000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:95832200-95834600	Enhancers	Dnd41	blood
5	chr4:95833000-95835600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr4:95833400-95836600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr4:95833600-95834000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:95833600-95834200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:95833600-95834200	Enhancers	Thymus	Thymus
10	chr4:95833600-95835000	Enhancers	Fetal Thymus	thymus
11	chr4:95833600-95835400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:95833600-95835400	Enhancers	Primary T cells from cord blood	blood
13	chr4:95833600-95835800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr4:95833800-95834200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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