Variant report

Variant	rs6537073
Chromosome Location	chr4:142722336-142722337
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10014610	0.89[ASN][1000 genomes]
rs10018460	0.89[ASN][1000 genomes]
rs10519610	0.86[JPT][hapmap]
rs10519625	0.89[ASN][1000 genomes]
rs12498901	0.86[JPT][hapmap]
rs12504148	0.86[JPT][hapmap]
rs12510514	0.86[JPT][hapmap]
rs1353033	0.89[ASN][1000 genomes]
rs1389099	0.89[ASN][1000 genomes]
rs1493015	0.89[ASN][1000 genomes]
rs1493019	0.89[ASN][1000 genomes]
rs1607595	0.86[JPT][hapmap]
rs17364630	0.86[JPT][hapmap]
rs1907948	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1987968	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2120050	0.89[ASN][1000 genomes]
rs28504216	0.98[ASN][1000 genomes]
rs28528751	0.94[ASN][1000 genomes]
rs4956405	0.86[JPT][hapmap]
rs4956413	0.89[ASN][1000 genomes]
rs6537074	0.89[ASN][1000 genomes]
rs6842735	0.86[JPT][hapmap]
rs6850492	0.86[JPT][hapmap]
rs7349640	0.86[JPT][hapmap]
rs7656341	0.89[ASN][1000 genomes]
rs7656958	0.89[ASN][1000 genomes]
rs7671458	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3401979	chr4:142434442-142803321	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1018949	chr4:142451823-142732365	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking 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	3 gene(s)	inside rSNPs	diseases
3	nsv1027004	chr4:142487721-143007320	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv830095	chr4:142695078-142884988	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142719600-142723000	Weak transcription	HSMM	muscle
2	chr4:142719800-142722400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:142719800-142723800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:142722200-142722600	Weak transcription	NHDF-Ad	bronchial

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