Variant report

Variant	rs6531992
Chromosome Location	chr4:76789516-76789517
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10007472	1.00[CHD][hapmap]
rs1021923	1.00[ASN][1000 genomes]
rs1021924	1.00[ASN][1000 genomes]
rs10856862	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11934786	1.00[ASN][1000 genomes]
rs11935735	1.00[ASN][1000 genomes]
rs13116352	1.00[ASN][1000 genomes]
rs13130621	1.00[CHD][hapmap];1.00[GIH][hapmap]
rs13149236	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1546567	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1546568	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1566975	1.00[GIH][hapmap]
rs17000735	1.00[EUR][1000 genomes]
rs17000764	1.00[EUR][1000 genomes]
rs17000810	1.00[EUR][1000 genomes]
rs17000961	0.83[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17000973	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17001036	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17001150	1.00[EUR][1000 genomes]
rs17001165	1.00[EUR][1000 genomes]
rs1847731	1.00[CHD][hapmap]
rs1972062	1.00[ASN][1000 genomes]
rs1972063	1.00[ASN][1000 genomes]
rs1976517	1.00[GIH][hapmap]
rs1983110	1.00[ASN][1000 genomes]
rs2047976	1.00[CHD][hapmap]
rs2174513	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2174514	1.00[ASN][1000 genomes]
rs2174515	1.00[ASN][1000 genomes]
rs28406977	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs324717	1.00[JPT][hapmap]
rs34155925	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3817099	1.00[CHD][hapmap]
rs4241572	1.00[ASN][1000 genomes]
rs4241573	1.00[ASN][1000 genomes]
rs4241574	1.00[CHD][hapmap];1.00[GIH][hapmap]
rs4241575	1.00[GIH][hapmap]
rs4288032	1.00[ASN][1000 genomes]
rs4324568	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4490489	1.00[ASN][1000 genomes]
rs4859410	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs4859563	0.85[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4859564	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs5015809	1.00[ASN][1000 genomes]
rs5028031	1.00[EUR][1000 genomes]
rs56024633	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57659593	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60044896	1.00[ASN][1000 genomes]
rs61288563	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6811934	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6824610	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6826893	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6838414	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6844961	1.00[EUR][1000 genomes]
rs6856987	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73825563	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73825569	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73825570	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7654738	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7668152	1.00[ASN][1000 genomes]
rs7668165	1.00[ASN][1000 genomes]
rs7669428	1.00[ASN][1000 genomes]
rs7685485	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7685710	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7691712	1.00[CHD][hapmap];1.00[GIH][hapmap]
rs7693116	1.00[EUR][1000 genomes]
rs7694386	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[ASN][1000 genomes]
rs9998204	0.82[ASW][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.98[MKK][hapmap];0.85[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3353539	chr4:76530136-76993859	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv529613	chr4:76654941-77081576	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 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	chr4:76782600-76789600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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