Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:110287703..110291909-chr4:110296308..110299506,3	K562	blood:

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10014623	0.97[EUR][1000 genomes]
rs10031251	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10031399	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10155246	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs10488879	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12641197	0.96[ASN][1000 genomes]
rs12641272	0.96[ASN][1000 genomes]
rs13126829	1.00[ASN][1000 genomes]
rs1557804	0.89[ASN][1000 genomes]
rs17842269	0.96[ASN][1000 genomes]
rs1859144	0.96[ASN][1000 genomes]
rs1859145	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1859146	0.89[ASN][1000 genomes]
rs1981541	0.81[ASN][1000 genomes]
rs2079107	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2214377	0.96[ASN][1000 genomes]
rs28463999	0.96[ASN][1000 genomes]
rs28542804	0.81[ASN][1000 genomes]
rs60369504	0.97[EUR][1000 genomes]
rs6825928	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6826161	1.00[CHB][hapmap]
rs730310	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7665024	1.00[ASN][1000 genomes]
rs7680752	0.89[ASN][1000 genomes]
rs7680920	0.89[ASN][1000 genomes]
rs7694523	1.00[ASN][1000 genomes]
rs7695754	1.00[JPT][hapmap]
rs7699247	0.81[ASN][1000 genomes]
rs9307329	0.96[ASN][1000 genomes]
rs9996537	0.96[ASN][1000 genomes]
rs9996920	0.96[ASN][1000 genomes]
rs9999270	0.96[ASN][1000 genomes]
rs9999278	0.96[ASN][1000 genomes]
rs9999751	0.96[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	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110286800-110288000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:110286800-110288000	Enhancers	NHEK	skin
3	chr4:110287000-110288000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:110287400-110288000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:110287400-110288000	Enhancers	Placenta	Placenta
6	chr4:110287600-110288800	Enhancers	HUVEC	blood vessel

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