Variant report

Variant	rs4442059
Chromosome Location	chr7:87704699-87704700
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:87702607..87705173-chr7:89180961..89183467,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10234048	0.81[CEU][hapmap]
rs10234412	0.81[CEU][hapmap]
rs1023538	0.86[EUR][1000 genomes]
rs10435251	0.88[ASN][1000 genomes]
rs10464571	0.81[EUR][1000 genomes]
rs10952913	0.92[CEU][hapmap]
rs11772873	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12535312	0.88[EUR][1000 genomes]
rs12535365	0.88[EUR][1000 genomes]
rs12537586	0.88[EUR][1000 genomes]
rs12671587	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12673545	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17339970	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2008834	0.92[CEU][hapmap]
rs2097918	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs2237541	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs2282951	0.88[ASN][1000 genomes]
rs2282955	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2282956	0.92[CEU][hapmap];0.88[EUR][1000 genomes]
rs2299199	0.88[CEU][hapmap]
rs2299200	0.92[CEU][hapmap]
rs3753103	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs4728731	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55637099	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56050913	0.89[ASN][1000 genomes]
rs56399147	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58850563	0.89[ASN][1000 genomes]
rs62486383	0.89[ASN][1000 genomes]
rs62486404	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62486407	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62486409	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6951172	0.81[CEU][hapmap]
rs6955696	0.92[CEU][hapmap]
rs6957754	0.80[EUR][1000 genomes]
rs6958024	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6968026	0.81[CEU][hapmap]
rs7777040	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7792853	0.80[EUR][1000 genomes]
rs7793308	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs7799148	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9632709	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1023352	chr7:87418818-88192925	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539005	chr7:87418818-88192925	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv525073	chr7:87535096-87812968	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4442059	ADAM22	cis	Muscle Skeletal	GTEx

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87701600-87704800	Enhancers	Fetal Lung	lung
2	chr7:87701600-87705000	Enhancers	Dnd41	blood
3	chr7:87702000-87705800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:87702200-87705800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:87702200-87706000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:87703000-87718800	Weak transcription	Brain Angular Gyrus	brain
7	chr7:87703800-87705000	Enhancers	Pancreatic Islets	Pancreatic Islet

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