Variant report

Variant	rs2727715
Chromosome Location	chr12:119668379-119668380
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1426624	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1465516	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2555287	0.92[CEU][hapmap];0.95[TSI][hapmap];0.94[EUR][1000 genomes]
rs2555288	0.89[EUR][1000 genomes]
rs2555289	0.96[EUR][1000 genomes]
rs2727708	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2727709	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2727710	0.82[CEU][hapmap];0.85[CHB][hapmap];0.84[CHD][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2727712	0.95[EUR][1000 genomes]
rs2727713	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2727714	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2727716	0.96[EUR][1000 genomes]
rs6490245	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv832528	chr12:119638211-119793401	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2727715	WSB2	cis	cerebellum	SCAN
rs2727715	PEX1	trans	cerebellum	SCAN
rs2727715	RNFT2	cis	parietal	SCAN

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119663600-119668800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:119664000-119676800	Weak transcription	Lung	lung
3	chr12:119667400-119669000	Enhancers	Primary hematopoietic stem cells	blood
4	chr12:119667600-119668400	Active TSS	A549	lung
5	chr12:119667600-119669200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:119667800-119668400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr12:119668000-119668400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr12:119668000-119669000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr12:119668200-119668800	Enhancers	K562	blood
10	chr12:119668200-119669000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr12:119668200-119669800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr12:119668200-119670000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr12:119668200-119670400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:119668200-119670400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr12:119668200-119672600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr12:119668200-119672600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr12:119668200-119672600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:119668200-119672600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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Input of quick search could be:

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

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