Variant report

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10489059	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs10489060	0.87[ASN][1000 genomes]
rs10489066	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs16893241	0.88[ASN][1000 genomes]
rs16893297	0.87[ASN][1000 genomes]
rs16893385	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs16893387	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs2215639	0.87[ASN][1000 genomes]
rs4574401	0.87[ASN][1000 genomes]
rs6851339	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6851785	0.92[ASN][1000 genomes]
rs73234692	0.92[ASN][1000 genomes]
rs73234694	0.90[ASN][1000 genomes]
rs73234696	0.88[ASN][1000 genomes]
rs73234701	0.88[ASN][1000 genomes]
rs73235977	0.87[ASN][1000 genomes]
rs73235978	0.87[ASN][1000 genomes]
rs73238006	0.87[ASN][1000 genomes]
rs73239725	0.87[ASN][1000 genomes]
rs73239734	0.87[ASN][1000 genomes]
rs73239736	0.83[ASN][1000 genomes]
rs73239739	0.87[ASN][1000 genomes]
rs73239740	0.87[ASN][1000 genomes]
rs73239743	0.87[ASN][1000 genomes]
rs73239747	0.87[ASN][1000 genomes]
rs73239749	0.87[ASN][1000 genomes]
rs73239751	0.87[ASN][1000 genomes]
rs73239758	0.87[ASN][1000 genomes]
rs73239760	0.87[ASN][1000 genomes]
rs73239761	0.85[ASN][1000 genomes]
rs73239765	0.87[ASN][1000 genomes]
rs73239766	0.87[ASN][1000 genomes]
rs73239768	0.87[ASN][1000 genomes]
rs73239769	0.87[ASN][1000 genomes]
rs73239771	0.87[ASN][1000 genomes]
rs73239772	0.87[ASN][1000 genomes]
rs73239773	0.87[ASN][1000 genomes]
rs73239774	0.87[ASN][1000 genomes]
rs73239777	0.87[ASN][1000 genomes]
rs7685190	0.87[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	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	nsv537047	chr4:16182060-16375787	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv537048	chr4:16226406-16375787	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr4:16258200-16278600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:16272600-16278600	Weak transcription	Adipose Nuclei	Adipose

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