Variant report

Variant	rs7825771
Chromosome Location	chr8:119554802-119554803
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10090804	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10097320	0.95[ASN][1000 genomes]
rs10104444	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10104761	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10110626	0.84[ASN][1000 genomes]
rs10111755	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10113428	0.82[ASN][1000 genomes]
rs11774748	0.92[ASN][1000 genomes]
rs11774993	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12541156	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12541178	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12545989	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12548521	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12549010	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12678125	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13269467	0.91[ASN][1000 genomes]
rs13278633	0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2515027	0.92[ASN][1000 genomes]
rs2515055	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2515056	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2515059	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs28574967	0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4327885	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4495457	0.81[ASN][1000 genomes]
rs4559272	0.82[ASN][1000 genomes]
rs4625062	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6469752	0.94[ASN][1000 genomes]
rs6469754	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6982778	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6984080	0.95[ASN][1000 genomes]
rs7004852	0.94[ASN][1000 genomes]
rs7012653	0.90[ASN][1000 genomes]
rs71505417	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7823933	0.94[ASN][1000 genomes]
rs7823939	0.94[ASN][1000 genomes]
rs7825490	0.93[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7826003	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7836391	0.92[ASN][1000 genomes]
rs9297589	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032681	chr8:119153316-119609948	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv539737	chr8:119153316-119609948	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv831443	chr8:119390590-119590662	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv6362	chr8:119554736-119599269	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119550600-119558800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr8:119550800-119558200	Weak transcription	Left Ventricle	heart
3	chr8:119551000-119555400	Weak transcription	GM12878-XiMat	blood
4	chr8:119554000-119560200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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