Variant report

Variant	rs7711707
Chromosome Location	chr5:59580296-59580297
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10461373	0.94[EUR][1000 genomes]
rs10461452	0.87[EUR][1000 genomes]
rs10461453	0.87[EUR][1000 genomes]
rs10514890	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10514891	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10514892	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10514895	0.89[EUR][1000 genomes]
rs12653662	0.85[EUR][1000 genomes]
rs12656804	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12656836	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12656871	0.87[EUR][1000 genomes]
rs12659623	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13158470	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13158573	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13159724	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13178509	0.89[EUR][1000 genomes]
rs13185075	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16877926	0.90[EUR][1000 genomes]
rs34114616	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34757284	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34762984	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35022567	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35250060	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35813355	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35955333	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4274945	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4276368	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4515249	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4700373	0.94[EUR][1000 genomes]
rs6880937	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71628002	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71630003	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71630005	0.94[EUR][1000 genomes]
rs7711621	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7718384	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7731452	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59559600-59584800	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59567400-59581600	Weak transcription	Fetal Brain Male	brain
3	chr5:59575400-59580800	Weak transcription	Aorta	Aorta
4	chr5:59577800-59581400	Weak transcription	HepG2	liver
5	chr5:59578600-59581600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:59579800-59581600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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