Variant report

Variant	rs9599533
Chromosome Location	chr13:70598508-70598509
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1441542	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1441561	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1441562	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs1470181	0.91[MEX][hapmap]
rs1596073	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs2033989	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2439610	0.91[MEX][hapmap]
rs2439612	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2439666	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2439667	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2472277	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2472280	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs2501204	0.81[CEU][hapmap];0.81[CHB][hapmap];0.81[CHD][hapmap]
rs6562606	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7332894	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9317864	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9529664	0.87[JPT][hapmap]
rs9542158	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9542159	0.88[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9542160	0.90[CEU][hapmap];0.84[CHB][hapmap];0.88[JPT][hapmap]
rs9542161	0.88[CEU][hapmap];0.88[CHB][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap]
rs9542164	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9572325	0.93[JPT][hapmap]
rs9592673	0.85[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs9599532	0.88[CEU][hapmap];0.88[CHB][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.91[TSI][hapmap];0.88[YRI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9989090	1.00[JPT][hapmap]
rs9989091	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530724	chr13:70393680-71164323	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1045918	chr13:70409675-70615997	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1038695	chr13:70484098-70654204	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv530606	chr13:70510296-70780461	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1051815	chr13:70570954-70736064	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv1844499	chr13:70578306-70884412	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv900494	chr13:70583646-70644890	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	esv2422425	chr13:70595689-70640062	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70595600-70602800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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