Variant report

Variant	rs17248550
Chromosome Location	chr4:91766611-91766612
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1115461	1.00[JPT][hapmap]
rs11946120	1.00[JPT][hapmap]
rs13108843	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13121860	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13128537	1.00[EUR][1000 genomes]
rs13132443	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13136325	1.00[JPT][hapmap]
rs34510263	1.00[EUR][1000 genomes]
rs35958829	1.00[ASN][1000 genomes]
rs7662582	1.00[EUR][1000 genomes];1.00[ASN][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	nsv534470	chr4:91342219-91842807	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv428766	chr4:91618397-91768647	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv879553	chr4:91691313-91868576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv879555	chr4:91743538-91967602	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv4422	chr4:91744177-91789188	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv491945	chr4:91753638-92240582	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr4:91752400-91775000	Weak transcription	Pancreas	Pancrea
2	chr4:91754600-91771400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:91765000-91768000	Weak transcription	HepG2	liver
4	chr4:91766000-91767400	Enhancers	A549	lung
5	chr4:91766200-91767400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr4:91766400-91767800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:91766600-91767200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:91766600-91767400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr4:91766600-91767400	Enhancers	HUVEC	blood vessel

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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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