Variant report

Variant	rs17108664
Chromosome Location	chr14:39442490-39442491
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10134656	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10139666	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10141079	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10141081	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10143720	0.81[ASN][1000 genomes]
rs10150756	0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10151124	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10151960	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1040680	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10467711	0.81[ASN][1000 genomes]
rs10483543	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11623907	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11623945	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11625689	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11627264	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11628480	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11628564	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11845793	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11848067	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12323565	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12590373	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17108576	0.84[ASN][1000 genomes]
rs17108596	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17108696	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1884384	0.89[CHB][hapmap]
rs1957065	0.82[ASN][1000 genomes]
rs2025061	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2144528	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28414518	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28470602	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3896147	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55672305	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55737943	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56064304	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56105133	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7144625	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7157092	0.88[ASN][1000 genomes]
rs7159520	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72669386	0.86[ASN][1000 genomes]
rs743223	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8019396	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs926970	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs993675	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3429206	chr14:39160730-39648836	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv901657	chr14:39410706-39460072	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1038622	chr14:39423562-39604035	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39441000-39442600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:39441000-39442600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:39442400-39442800	Enhancers	HepG2	liver
4	chr14:39442400-39443000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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