Variant report

Variant	rs13024879
Chromosome Location	chr2:141639106-141639107
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10185560	1.00[CHB][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10189583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10194398	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10496855	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12472481	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12691580	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12987572	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12989752	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12993423	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12999130	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13001345	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13006054	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13007335	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13007422	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13013928	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13021153	1.00[ASN][1000 genomes]
rs13022675	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13026491	1.00[ASN][1000 genomes]
rs1429346	1.00[CHB][hapmap]
rs17518049	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1963862	0.82[EUR][1000 genomes]
rs2380945	1.00[CHB][hapmap]
rs34386576	0.93[ASN][1000 genomes]
rs67402821	1.00[ASN][1000 genomes]
rs7562670	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1003008	chr2:141518795-141763505	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141638400-141639800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:141638400-141639800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:141638400-141640000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:141639000-141640200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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