Variant report

Variant	rs17567259
Chromosome Location	chr1:75693132-75693133
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10493560	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10493563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493567	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap]
rs10493568	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs10493572	1.00[CHB][hapmap]
rs11162740	1.00[ASN][1000 genomes]
rs11162743	1.00[ASN][1000 genomes]
rs11162745	1.00[ASN][1000 genomes]
rs11162747	1.00[ASN][1000 genomes]
rs11162748	1.00[ASN][1000 genomes]
rs12077329	1.00[ASN][1000 genomes]
rs12085115	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs12087682	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12405357	1.00[CHB][hapmap]
rs12408190	1.00[CHB][hapmap]
rs12408827	1.00[CHB][hapmap]
rs12411159	1.00[CHB][hapmap]
rs1249664	1.00[CHB][hapmap]
rs1249666	1.00[CHB][hapmap]
rs1249667	1.00[CHB][hapmap]
rs1262045	1.00[CHB][hapmap]
rs1526515	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17096320	1.00[ASN][1000 genomes]
rs17096323	1.00[ASN][1000 genomes]
rs17096324	1.00[ASN][1000 genomes]
rs17096342	1.00[ASN][1000 genomes]
rs17096353	1.00[ASN][1000 genomes]
rs17096388	1.00[ASN][1000 genomes]
rs17096391	1.00[ASN][1000 genomes]
rs17096399	1.00[ASN][1000 genomes]
rs17096401	1.00[ASN][1000 genomes]
rs17096406	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17096504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17096776	1.00[CHB][hapmap]
rs17096782	1.00[CHB][hapmap]
rs17097953	1.00[CHB][hapmap]
rs17097955	1.00[CHB][hapmap]
rs17567748	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17584320	1.00[CHB][hapmap]
rs17644957	1.00[CHB][hapmap]
rs1876035	1.00[ASN][1000 genomes]
rs1913118	1.00[CHB][hapmap]
rs1936359	1.00[CHB][hapmap]
rs2221458	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs28817923	1.00[ASN][1000 genomes]
rs28856993	1.00[ASN][1000 genomes]
rs4540592	1.00[CHB][hapmap]
rs5021868	1.00[ASN][1000 genomes]
rs60651982	1.00[ASN][1000 genomes]
rs983331	1.00[CHB][hapmap]

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	nsv871743	chr1:75235082-75714554	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv3368999	chr1:75524762-75933220	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr1:75676400-75700400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:75678800-75705400	Weak transcription	Fetal Brain Female	brain
3	chr1:75685200-75700200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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