Variant report

Variant	rs7696111
Chromosome Location	chr4:166276414-166276415
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10015275	0.91[EUR][1000 genomes]
rs10021532	0.89[EUR][1000 genomes]
rs10025377	0.91[EUR][1000 genomes]
rs10031858	0.89[EUR][1000 genomes]
rs11100607	0.84[EUR][1000 genomes]
rs11940090	0.82[ASN][1000 genomes]
rs12506365	0.82[ASN][1000 genomes]
rs13106028	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13137171	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17046337	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17046351	0.93[EUR][1000 genomes]
rs17585655	0.87[EUR][1000 genomes]
rs17585739	0.87[EUR][1000 genomes]
rs28484900	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28735257	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4690813	0.82[ASN][1000 genomes]
rs4691187	0.82[ASN][1000 genomes]
rs6536907	0.82[ASN][1000 genomes]
rs6536908	0.82[ASN][1000 genomes]
rs6536909	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6817186	0.89[EUR][1000 genomes]
rs6842704	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6846664	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6853552	0.93[EUR][1000 genomes]
rs72701627	0.86[EUR][1000 genomes]
rs72701628	0.87[EUR][1000 genomes]
rs72701629	0.87[EUR][1000 genomes]
rs72701630	0.87[EUR][1000 genomes]
rs72701632	0.89[EUR][1000 genomes]
rs72701634	0.89[EUR][1000 genomes]
rs72701636	0.89[EUR][1000 genomes]
rs72701637	0.93[EUR][1000 genomes]
rs72701639	0.93[EUR][1000 genomes]
rs72701642	0.93[EUR][1000 genomes]
rs72701645	0.93[EUR][1000 genomes]
rs72701652	0.91[EUR][1000 genomes]
rs72701657	0.93[EUR][1000 genomes]
rs72701659	0.93[EUR][1000 genomes]
rs72701664	0.93[EUR][1000 genomes]
rs7656675	0.93[EUR][1000 genomes]
rs7657847	0.93[EUR][1000 genomes]
rs7671176	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7677572	0.82[ASN][1000 genomes]
rs7679322	0.82[EUR][1000 genomes]
rs7679808	0.87[EUR][1000 genomes]
rs934814	0.82[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	esv1847399	chr4:166259587-166284836	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166263200-166280400	Weak transcription	Adipose Nuclei	Adipose
2	chr4:166270000-166276800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:166273200-166276600	Weak transcription	HepG2	liver
4	chr4:166275400-166277000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr4:166275600-166277000	Weak transcription	Primary monocytes fromperipheralblood	blood

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