Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10009182	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10517708	1.00[ASN][1000 genomes]
rs12498243	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1379604	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1379605	1.00[ASN][1000 genomes]
rs1457812	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1457813	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1457814	0.83[AMR][1000 genomes]
rs1902828	0.94[ASN][1000 genomes]
rs2088980	0.83[AMR][1000 genomes]
rs2348622	1.00[ASN][1000 genomes]
rs4596201	0.94[ASN][1000 genomes]
rs4690956	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4691610	0.94[ASN][1000 genomes]
rs6816178	0.83[AMR][1000 genomes]
rs6847951	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6849563	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs72971116	0.83[AMR][1000 genomes]
rs72971126	0.83[AMR][1000 genomes]
rs72971147	0.83[AMR][1000 genomes]
rs72982005	0.83[AMR][1000 genomes]
rs7675486	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs991839	1.00[ASN][1000 genomes]
rs991840	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[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	nsv1015469	chr4:160389277-160841619	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537316	chr4:160389277-160841619	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160685200-160687400	Enhancers	HSMM	muscle
2	chr4:160685200-160687600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:160685200-160689800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr4:160685400-160686200	Enhancers	Fetal Brain Male	brain
5	chr4:160685400-160689600	Enhancers	NH-A	brain
6	chr4:160685600-160687000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:160685800-160686200	Enhancers	Rectal Smooth Muscle	rectum
8	chr4:160686000-160687200	Weak transcription	HSMMtube	muscle
9	chr4:160686000-160691800	Weak transcription	Colon Smooth Muscle	Colon
10	chr4:160686200-160687200	Weak transcription	Fetal Brain Male	brain
11	chr4:160686200-160692200	Weak transcription	Rectal Smooth Muscle	rectum

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