Variant report

Variant	rs9691240
Chromosome Location	chr7:87752241-87752242
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10227241	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10229877	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10234048	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10234412	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10272494	0.87[ASN][1000 genomes]
rs10281274	0.96[ASN][1000 genomes]
rs10952910	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10952911	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10952914	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11770825	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12540117	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12670301	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13245213	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2008840	0.82[EUR][1000 genomes]
rs2237540	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2282957	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2299199	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2301998	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3753105	0.86[EUR][1000 genomes]
rs3753106	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4727151	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4727152	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61598739	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62486408	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6465129	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6951172	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6955194	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6964103	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6968026	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6971348	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs726328	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7793051	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9632709	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9641023	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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
rs9691240	ADAM22	cis	Muscle Skeletal	GTEx

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87741200-87782600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:87743400-87761800	Weak transcription	GM12878-XiMat	blood
3	chr7:87745000-87756600	Weak transcription	Fetal Intestine Small	intestine

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