Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10088416	0.81[AFR][1000 genomes]
rs10094550	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10095049	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10808879	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10958352	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11992913	0.82[AFR][1000 genomes]
rs28497511	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs59824595	0.81[AFR][1000 genomes]
rs59876580	0.83[AFR][1000 genomes]
rs61666049	0.81[AFR][1000 genomes]
rs6473807	0.81[AFR][1000 genomes]
rs6473822	0.87[CEU][hapmap]
rs6981186	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6984000	0.82[AFR][1000 genomes]
rs6988566	0.81[AFR][1000 genomes]
rs6994070	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7011197	0.81[AFR][1000 genomes]
rs7011684	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7015924	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7016942	0.82[AFR][1000 genomes]
rs7017919	0.82[AFR][1000 genomes]
rs73588563	0.81[AMR][1000 genomes]
rs7461559	0.81[AFR][1000 genomes]
rs7463912	0.81[AMR][1000 genomes]
rs7813768	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7816572	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7817965	0.81[ASN][1000 genomes]
rs7818414	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7840171	0.83[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs7841400	0.85[AFR][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	nsv1016224	chr8:53719941-54367534	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv530534	chr8:53787984-54367353	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3377304	chr8:53873441-54380875	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv2752674	chr8:54181147-54483747	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr8:54274200-54278800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:54274400-54278800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:54275400-54281200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:54277000-54278200	Weak transcription	Fetal Brain Female	brain

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