Variant report

Variant	rs6469963
Chromosome Location	chr8:121908427-121908428
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10094772	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10096496	0.93[EUR][1000 genomes]
rs10111219	0.92[EUR][1000 genomes]
rs11989426	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13270830	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13277545	0.82[EUR][1000 genomes]
rs13279396	0.82[EUR][1000 genomes]
rs28490321	0.93[EUR][1000 genomes]
rs2891944	1.00[CEU][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.92[EUR][1000 genomes]
rs2891945	0.93[EUR][1000 genomes]
rs35587464	0.89[CEU][hapmap]
rs4507806	0.81[EUR][1000 genomes]
rs57231964	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57431019	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6469959	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6469960	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6469961	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6469962	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7001670	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7010909	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7016191	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7820673	0.86[EUR][1000 genomes]
rs7841441	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016172	chr8:121679590-121929916	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv891423	chr8:121847643-121994660	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv465790	chr8:121853405-122185415	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv612114	chr8:121853405-122185415	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv891425	chr8:121875083-122025559	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121907200-121913200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:121908200-121909000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr8:121908400-121908600	Enhancers	Psoas Muscle	Psoas
4	chr8:121908400-121909000	ZNF genes & repeats	Aorta	Aorta

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