Variant report

Variant	rs7151991
Chromosome Location	chr14:32635572-32635573
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17478241	0.83[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1958366	0.82[GIH][hapmap]
rs35517039	0.82[AMR][1000 genomes]
rs6571497	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7152756	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7153052	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8004917	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9332386	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832764	chr14:32564468-32723213	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32624200-32636800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr14:32624200-32637000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:32624200-32638400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr14:32625200-32637000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr14:32626400-32637400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr14:32626600-32638200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:32626800-32637000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:32635000-32635800	Enhancers	GM12878-XiMat	blood
9	chr14:32635000-32636000	Enhancers	Primary B cells from peripheral blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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