Variant report

Variant	rs4653863
Chromosome Location	chr1:223862733-223862734
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10495210	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10495212	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10799570	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10915972	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10916633	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1109222	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1125346	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12408619	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12566877	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16842027	0.90[EUR][1000 genomes]
rs2186009	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34089008	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4653518	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4653520	0.86[EUR][1000 genomes]
rs4653523	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4653859	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4653868	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4653870	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4653877	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57611697	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs60773808	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61825220	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6661481	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6671050	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6677146	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6687391	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6687688	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6691383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6691396	0.90[EUR][1000 genomes]
rs6693911	0.81[AMR][1000 genomes]
rs6701150	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs68072917	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72629690	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72629691	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7549550	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832681	chr1:223698048-224002691	Strong transcription Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv873211	chr1:223707647-223867631	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3361888	chr1:223725597-224114846	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1007380	chr1:223834380-224042190	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv535310	chr1:223834380-224042190	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	esv34082	chr1:223851018-224144509	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223855800-223865800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:223861800-223863000	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr1:223861800-223863200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr1:223862400-223866200	Weak transcription	Spleen	Spleen
5	chr1:223862400-223869800	Weak transcription	Pancreas	Pancrea

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