Variant report

Variant	rs7856523
Chromosome Location	chr9:15528418-15528419
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr9:15528357-15528474	NB4	blood:	n/a	chr9:15528425-15528435
2	USF2	chr9:15528321-15528430	GM12878	blood:	n/a	n/a
3	MAX	chr9:15528381-15528547	NB4	blood:	n/a	chr9:15528425-15528435
4	NRF1	chr9:15528305-15528424	GM12878	blood:	n/a	n/a
5	MYC	chr9:15528374-15528510	K562	blood:	n/a	chr9:15528425-15528435

Variant related genes	Relation type
RN7SL98P	TF binding region
FTH1P12	TF binding region

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1057644	1.00[ASN][1000 genomes]
rs1057645	1.00[ASN][1000 genomes]
rs1057646	1.00[ASN][1000 genomes]
rs10810392	0.84[AFR][1000 genomes]
rs10810393	0.83[AFR][1000 genomes]
rs10810394	0.84[AFR][1000 genomes]
rs12001969	1.00[ASN][1000 genomes]
rs12002581	1.00[ASN][1000 genomes]
rs12003712	1.00[ASN][1000 genomes]
rs16933257	1.00[ASN][1000 genomes]
rs16933296	0.81[EUR][1000 genomes]
rs16933332	1.00[ASN][1000 genomes]
rs16933350	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3087653	0.85[EUR][1000 genomes]
rs41268961	0.85[EUR][1000 genomes]
rs41306098	0.85[EUR][1000 genomes]
rs57900433	1.00[ASN][1000 genomes]
rs58168894	0.90[AFR][1000 genomes]
rs59355275	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59520337	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62570969	0.81[EUR][1000 genomes]
rs62570972	0.81[EUR][1000 genomes]
rs62570976	0.80[EUR][1000 genomes]
rs62570980	0.85[EUR][1000 genomes]
rs62570991	0.85[EUR][1000 genomes]
rs62570992	0.85[EUR][1000 genomes]
rs62570993	0.85[EUR][1000 genomes]
rs62571001	0.81[EUR][1000 genomes]
rs62571002	0.81[EUR][1000 genomes]
rs62571003	0.83[EUR][1000 genomes]
rs62571007	0.85[EUR][1000 genomes]
rs62571008	0.83[EUR][1000 genomes]
rs62571009	0.85[EUR][1000 genomes]
rs62571011	0.85[EUR][1000 genomes]
rs62571015	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62571016	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62571017	0.95[EUR][1000 genomes]
rs62571018	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62571029	0.90[EUR][1000 genomes]
rs62571033	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62571037	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62571046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62571047	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62571048	1.00[EUR][1000 genomes]
rs62571050	0.92[EUR][1000 genomes]
rs62571051	0.90[EUR][1000 genomes]
rs62571052	0.87[EUR][1000 genomes]
rs7032720	1.00[ASN][1000 genomes]
rs72704750	1.00[ASN][1000 genomes]
rs73410204	0.95[AFR][1000 genomes]
rs73410215	0.90[AFR][1000 genomes]
rs73423305	1.00[ASN][1000 genomes]
rs7856486	1.00[ASN][1000 genomes]
rs7856657	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7858863	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	nsv517975	chr9:15286446-15534070	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv892629	chr9:15516375-15634326	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7856523	PSIP1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15528400-15528800	Enhancers	GM12878-XiMat	blood

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