Variant report

Variant	rs35787624
Chromosome Location	chr2:76389335-76389336
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:76388397..76390343-chr2:76392560..76394463,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10168901	0.84[ASN][1000 genomes]
rs10188424	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10205242	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11673856	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11678895	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11679728	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11690678	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12713863	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12987316	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12996043	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12997508	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13002280	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13030138	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13409722	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1608587	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17700671	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17750689	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17750877	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1916870	0.84[ASN][1000 genomes]
rs34236297	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34743837	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35475961	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35861585	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6547046	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67496128	0.96[EUR][1000 genomes]
rs6761061	0.84[ASN][1000 genomes]
rs68152182	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71418796	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71418798	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71420904	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs744235	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7565818	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7572341	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs997292	0.84[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	nsv834265	chr2:76275611-76450728	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv999645	chr2:76317006-76451354	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76385800-76389400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:76386000-76389400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:76389200-76389400	Enhancers	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links