Variant report

Variant	rs60064586
Chromosome Location	chr8:54239490-54239491
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10088416	1.00[ASN][1000 genomes]
rs10091452	1.00[ASN][1000 genomes]
rs10092984	1.00[ASN][1000 genomes]
rs10094550	1.00[ASN][1000 genomes]
rs10094903	1.00[ASN][1000 genomes]
rs10095049	1.00[ASN][1000 genomes]
rs10101249	1.00[ASN][1000 genomes]
rs10958352	0.84[ASN][1000 genomes]
rs11985025	0.84[AMR][1000 genomes]
rs11989664	0.85[AMR][1000 genomes]
rs11990775	1.00[ASN][1000 genomes]
rs11992913	1.00[ASN][1000 genomes]
rs11995645	0.85[AMR][1000 genomes]
rs2376417	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28368546	0.93[ASN][1000 genomes]
rs28497511	0.98[ASN][1000 genomes]
rs4131126	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55692942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56688789	0.99[ASN][1000 genomes]
rs58107215	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58363137	0.84[AMR][1000 genomes]
rs59824595	1.00[ASN][1000 genomes]
rs59876580	0.93[ASN][1000 genomes]
rs61666049	1.00[ASN][1000 genomes]
rs6473802	0.91[ASN][1000 genomes]
rs6473803	0.88[ASN][1000 genomes]
rs6473804	0.91[ASN][1000 genomes]
rs6473805	0.91[ASN][1000 genomes]
rs6473806	0.91[ASN][1000 genomes]
rs6473807	0.98[ASN][1000 genomes]
rs6981186	1.00[ASN][1000 genomes]
rs6983218	0.86[ASN][1000 genomes]
rs6984000	1.00[ASN][1000 genomes]
rs6988566	1.00[ASN][1000 genomes]
rs6988589	0.97[ASN][1000 genomes]
rs6990680	1.00[ASN][1000 genomes]
rs6991236	0.93[ASN][1000 genomes]
rs6991600	0.92[ASN][1000 genomes]
rs6991749	0.92[ASN][1000 genomes]
rs6994070	1.00[ASN][1000 genomes]
rs6996899	1.00[ASN][1000 genomes]
rs7001899	0.86[ASN][1000 genomes]
rs7011197	1.00[ASN][1000 genomes]
rs7011684	1.00[ASN][1000 genomes]
rs7015924	1.00[ASN][1000 genomes]
rs7016942	1.00[ASN][1000 genomes]
rs7017919	1.00[ASN][1000 genomes]
rs73588563	1.00[ASN][1000 genomes]
rs73679713	0.84[AMR][1000 genomes]
rs73679716	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73679730	0.84[AMR][1000 genomes]
rs7461559	1.00[ASN][1000 genomes]
rs7462232	0.84[AMR][1000 genomes]
rs7463912	1.00[ASN][1000 genomes]
rs7465082	0.85[AMR][1000 genomes]
rs7813768	0.98[ASN][1000 genomes]
rs7814249	1.00[ASN][1000 genomes]
rs7816572	0.98[ASN][1000 genomes]
rs7817965	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7818414	1.00[ASN][1000 genomes]
rs7839485	0.85[AMR][1000 genomes]
rs7840171	0.95[ASN][1000 genomes]
rs7841400	1.00[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	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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54239000-54242400	Weak transcription	Brain Germinal Matrix	brain

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