Variant report

Variant	rs17796693
Chromosome Location	chr14:85740061-85740062
allele	C/T
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:15)

rs_ID	r²[population]
rs10498583	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11626130	0.84[GIH][hapmap]
rs12897361	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1767418	0.81[CEU][hapmap]
rs17796669	0.82[CHB][hapmap]
rs1867082	1.00[CHB][hapmap]
rs34144829	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34880356	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34980802	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs36073512	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7160419	0.82[CHB][hapmap]
rs8008508	0.91[ASN][1000 genomes]
rs8008671	0.95[EUR][1000 genomes]
rs8009290	0.91[ASN][1000 genomes]
rs8013627	0.91[EUR][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	chr14:85739000-85740800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:85740000-85740200	Enhancers	HUVEC	blood vessel
3	chr14:85740000-85740600	Enhancers	Adipose Derived Mesenchymal Stem Cell 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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