Variant report

Variant	rs6826793
Chromosome Location	chr4:16381549-16381550
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10026585	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1005391	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1005392	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1125986	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12499039	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12501291	1.00[JPT][hapmap]
rs12511340	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13434764	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16893390	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16893392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16893432	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17562392	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17563394	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs203441	1.00[CEU][hapmap]
rs2215641	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28479363	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28660004	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57320479	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58630466	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58854692	0.89[EUR][1000 genomes]
rs62289023	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62298775	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62298783	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7660122	0.89[CEU][hapmap];0.88[JPT][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9654127	0.89[EUR][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	nsv1004821	chr4:16055996-16830629	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv537046	chr4:16055996-16830629	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1006449	chr4:16338191-16412544	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428755	chr4:16366311-16528135	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16381000-16382000	Enhancers	Fetal Kidney	kidney
2	chr4:16381200-16384400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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