Variant report

Variant	rs8023607
Chromosome Location	chr15:62121608-62121609
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12438629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12442569	0.86[GIH][hapmap];1.00[TSI][hapmap]
rs12594218	0.88[EUR][1000 genomes]
rs12595158	0.81[GIH][hapmap]
rs17238189	0.86[GIH][hapmap];1.00[TSI][hapmap]
rs3784635	0.86[GIH][hapmap];1.00[TSI][hapmap]
rs4775452	0.86[GIH][hapmap];1.00[TSI][hapmap]
rs8033347	0.88[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62121000-62122000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr15:62121000-62122000	Bivalent Enhancer	Fetal Stomach	stomach
3	chr15:62121200-62122000	Enhancers	Adipose Nuclei	Adipose
4	chr15:62121400-62121800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr15:62121400-62121800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr15:62121400-62122200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr15:62121600-62122000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:62121600-62122000	Weak transcription	Right Atrium	heart

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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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