Variant report

Variant	rs6878888
Chromosome Location	chr5:114408501-114408502
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10055823	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10061081	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10061288	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10077885	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10078015	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10477526	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11241305	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1446074	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1838747	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2121188	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2921618	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2921625	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2921626	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2921629	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2974505	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2974506	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2974507	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2974516	0.89[ASN][1000 genomes]
rs2974609	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2974610	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2974612	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4073838	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4073839	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4075509	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4075510	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4076057	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4131436	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4131437	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4235764	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4235765	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4235768	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4235769	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4235770	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4286654	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4312873	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4360034	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4382158	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4392610	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4421095	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4435857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4485921	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4485922	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4489055	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4554207	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4705720	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6869551	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7722841	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs966791	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	esv2763486	chr5:114406248-114409476	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114407400-114409000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:114407600-114408800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:114407600-114409200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr5:114407800-114409000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr5:114407800-114409400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr5:114408000-114408800	Enhancers	Primary B cells from peripheral blood	blood
7	chr5:114408000-114408800	Enhancers	Esophagus	oesophagus
8	chr5:114408000-114409000	Enhancers	H1 Cell Line	embryonic stem cell
9	chr5:114408000-114409200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr5:114408000-114409200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr5:114408000-114409200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:114408200-114408800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr5:114408200-114408800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr5:114408200-114409000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr5:114408400-114408600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:114408400-114408800	Weak transcription	Fetal Brain Male	brain
17	chr5:114408400-114409000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr5:114408400-114409200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr5:114408400-114409200	Enhancers	Brain Germinal Matrix	brain

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