Variant report

Variant	rs11982510
Chromosome Location	chr7:119949168-119949169
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10239849	0.83[CEU][hapmap]
rs10488286	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10488289	0.83[CEU][hapmap]
rs10488290	0.83[CEU][hapmap]
rs10488293	0.91[CEU][hapmap]
rs10953909	0.91[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs10953911	0.83[CEU][hapmap]
rs11487122	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs11760262	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11762819	0.81[CEU][hapmap]
rs11763966	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11765076	0.83[CEU][hapmap]
rs11767260	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs11767585	0.85[CHB][hapmap]
rs11768610	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs11769050	0.83[CEU][hapmap]
rs11769340	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11769783	0.83[CEU][hapmap]
rs11773232	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11970921	0.81[CEU][hapmap]
rs11972808	0.83[CEU][hapmap]
rs17323760	0.82[EUR][1000 genomes]
rs17323788	0.91[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs17324055	0.83[CEU][hapmap]
rs17324726	0.83[CEU][hapmap]
rs17374849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17376905	0.83[CEU][hapmap]
rs17376968	0.83[CEU][hapmap]
rs17594101	0.94[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs17594220	0.93[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs34850246	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4140688	0.82[EUR][1000 genomes]
rs55680276	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55963403	0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs56244901	0.90[ASN][1000 genomes]
rs56967206	0.84[EUR][1000 genomes]
rs62469500	0.83[ASN][1000 genomes]
rs62469501	0.83[ASN][1000 genomes]
rs62469503	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs62469505	0.90[ASN][1000 genomes]
rs62469506	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs62469507	0.90[ASN][1000 genomes]
rs62470461	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62470532	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62470539	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62470541	0.84[EUR][1000 genomes]
rs62470545	0.83[EUR][1000 genomes]
rs62470547	0.84[EUR][1000 genomes]
rs62470548	0.84[EUR][1000 genomes]
rs62470550	0.83[EUR][1000 genomes]
rs6466742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6942451	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6942755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6969916	0.90[ASN][1000 genomes]
rs6978586	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs73213448	0.83[ASN][1000 genomes]
rs73213458	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs736612	0.91[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs7777091	0.83[ASN][1000 genomes]
rs7778213	0.91[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs7786492	0.83[ASN][1000 genomes]
rs7794826	0.83[CEU][hapmap]
rs7800545	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7809257	0.83[CEU][hapmap]
rs917901	0.83[CEU][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	nsv608326	chr7:119828331-119995890	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv3440176	chr7:119949038-119949526	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119939400-119995600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:119948600-119949200	Weak transcription	GM12878-XiMat	blood
3	chr7:119948800-119955400	Weak transcription	HUES64 Cell Line	embryonic stem cell

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