Variant report

Variant	rs8008508
Chromosome Location	chr14:85744004-85744005
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10498583	0.96[ASN][1000 genomes]
rs12435282	0.98[EUR][1000 genomes]
rs17796669	0.85[CHB][hapmap]
rs17796693	0.91[ASN][1000 genomes]
rs1867082	1.00[CHB][hapmap]
rs34144829	0.88[ASN][1000 genomes]
rs34880356	0.88[ASN][1000 genomes]
rs34980802	0.81[ASN][1000 genomes]
rs36073512	0.91[ASN][1000 genomes]
rs7160419	0.85[CHB][hapmap]
rs8009290	0.80[EUR][1000 genomes];1.00[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	esv2422273	chr14:85703149-85767292	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85740600-85745600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr14:85743200-85744600	Enhancers	Fetal Brain Male	brain
3	chr14:85743800-85750200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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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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