Variant report

Variant	rs1587121
Chromosome Location	chr4:21405662-21405663
allele	C/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:38)

rs_ID	r²[population]
rs10516383	0.93[JPT][hapmap]
rs10516384	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs11933121	0.93[JPT][hapmap]
rs11935013	0.87[EUR][1000 genomes]
rs13117744	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs13124591	0.93[JPT][hapmap];0.87[EUR][1000 genomes]
rs13129012	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13130239	0.85[JPT][hapmap]
rs13133567	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs13137692	0.80[JPT][hapmap]
rs13141449	0.86[JPT][hapmap]
rs13141872	0.93[JPT][hapmap]
rs1485513	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870851	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870854	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs16870857	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870858	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870860	0.85[JPT][hapmap]
rs16870863	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870865	1.00[GIH][hapmap];0.93[JPT][hapmap]
rs16870875	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870886	0.93[JPT][hapmap]
rs16870888	0.93[JPT][hapmap]
rs16870895	0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870905	1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap]
rs16870916	0.87[EUR][1000 genomes]
rs16870934	0.93[JPT][hapmap];0.87[EUR][1000 genomes]
rs16870966	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16871003	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1872457	0.92[JPT][hapmap]
rs2323002	0.84[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap]
rs36012574	0.87[EUR][1000 genomes]
rs4352463	0.84[CHD][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];1.00[TSI][hapmap]
rs4696978	0.89[AMR][1000 genomes]
rs71607070	0.87[EUR][1000 genomes]
rs71607071	0.87[EUR][1000 genomes]
rs71607073	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7698713	0.93[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014062	chr4:21270358-21479027	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1005453	chr4:21295066-21454143	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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