Variant report

Variant	rs6881511
Chromosome Location	chr5:106555504-106555505
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11242632	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12522490	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12522515	0.89[EUR][1000 genomes]
rs1345637	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1363311	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2410946	0.89[EUR][1000 genomes]
rs2410952	0.89[EUR][1000 genomes]
rs2410979	0.85[ASN][1000 genomes]
rs4143065	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4245993	0.88[EUR][1000 genomes]
rs4572985	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4631165	0.85[EUR][1000 genomes]
rs4957690	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55689542	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56255936	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6596720	0.85[EUR][1000 genomes]
rs6596722	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6596730	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6871050	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6871532	0.87[EUR][1000 genomes]
rs6878038	0.87[EUR][1000 genomes]
rs6888773	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6892104	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7706390	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7710297	0.89[EUR][1000 genomes]
rs7710569	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7733658	0.89[EUR][1000 genomes]
rs7736860	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv823170	chr5:106326293-106673695	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2752056	chr5:106422649-106563101	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv882680	chr5:106493350-106573961	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv882681	chr5:106508913-106573961	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106551800-106557200	Weak transcription	Right Ventricle	heart
2	chr5:106552600-106557200	Weak transcription	Lung	lung
3	chr5:106555400-106556600	Enhancers	Fetal Heart	heart

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