Variant report

Variant	rs4082258
Chromosome Location	chr8:67198497-67198498
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:67187465..67190197-chr8:67197667..67200205,2	K562	blood:
2	chr8:67196893..67200364-chr8:67203105..67206589,3	K562	blood:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10092496	0.90[EUR][1000 genomes]
rs10092723	0.90[EUR][1000 genomes]
rs10096645	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11775119	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11775572	0.90[EUR][1000 genomes]
rs11777492	0.89[EUR][1000 genomes]
rs11780222	0.95[EUR][1000 genomes]
rs11782482	0.90[EUR][1000 genomes]
rs11997309	0.90[EUR][1000 genomes]
rs11998196	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16932761	0.90[EUR][1000 genomes]
rs2357825	0.89[EUR][1000 genomes]
rs28877929	0.87[EUR][1000 genomes]
rs4082259	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4147353	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4269528	0.90[EUR][1000 genomes]
rs4543527	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4737774	0.82[EUR][1000 genomes]
rs4737775	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4737776	0.90[EUR][1000 genomes]
rs4737777	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4737779	0.96[EUR][1000 genomes]
rs6987662	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6989260	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6998504	0.91[EUR][1000 genomes]
rs7006364	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7010589	0.85[EUR][1000 genomes]
rs9298111	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9694332	0.96[EUR][1000 genomes];0.81[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	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3414665	chr8:66936816-67381935	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv1017345	chr8:67184975-67209954	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv6235	chr8:67188081-67232737	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67194200-67203800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:67197800-67198800	Weak transcription	Right Ventricle	heart
3	chr8:67197800-67199000	Weak transcription	Fetal Muscle Trunk	muscle

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