Variant report

Variant	rs58895605
Chromosome Location	chr15:54791127-54791128
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1858351	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1858352	0.88[AMR][1000 genomes]
rs56696332	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs57226140	0.81[ASN][1000 genomes]
rs58025043	1.00[AFR][1000 genomes]
rs60172465	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs62022398	1.00[AFR][1000 genomes]
rs62022401	1.00[AFR][1000 genomes]
rs62022405	1.00[AFR][1000 genomes]
rs62022406	1.00[AFR][1000 genomes]
rs62022409	1.00[AFR][1000 genomes]
rs62022411	1.00[AFR][1000 genomes]
rs62022413	1.00[AFR][1000 genomes]
rs62022414	1.00[AFR][1000 genomes]
rs62022419	1.00[AFR][1000 genomes]
rs72734781	0.81[ASN][1000 genomes]
rs72734791	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv904233	chr15:54703195-54797177	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv457153	chr15:54705902-54795040	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv569504	chr15:54705902-54795040	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv904235	chr15:54710873-54795040	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv569506	chr15:54715550-54796592	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1038660	chr15:54756184-55039913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54775200-54794000	Weak transcription	Fetal Lung	lung
2	chr15:54777800-54810400	Weak transcription	Aorta	Aorta
3	chr15:54785600-54791200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:54787000-54791200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:54789800-54791400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:54790800-54793200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr15:54790800-54793200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr15:54791000-54792600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr15:54791000-54793000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr15:54791000-54793200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:54791000-54793200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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