Variant report

Variant	rs12657771
Chromosome Location	chr5:36787962-36787963
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs13158310	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13170811	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13180309	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1466862	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs150380	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs151944	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs158622	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs158623	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs158624	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs158791	0.90[ASN][1000 genomes]
rs158796	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs158803	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs159749	0.84[ASN][1000 genomes]
rs159751	0.83[ASN][1000 genomes]
rs159753	0.85[ASN][1000 genomes]
rs159755	0.86[ASN][1000 genomes]
rs168662	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs184182	0.85[ASN][1000 genomes]
rs292182	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs292183	0.89[ASN][1000 genomes]
rs292184	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs292194	0.86[ASN][1000 genomes]
rs292195	0.90[ASN][1000 genomes]
rs296962	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs300060	0.84[ASN][1000 genomes]
rs300061	0.84[ASN][1000 genomes]
rs300063	0.84[ASN][1000 genomes]
rs300064	0.83[ASN][1000 genomes]
rs300065	0.86[ASN][1000 genomes]
rs3104057	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6899155	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[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	nsv492319	chr5:36570707-37061019	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv527961	chr5:36781051-36828730	Enhancers Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	1 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	chr5:36786000-36788000	Enhancers	Duodenum Mucosa	Duodenum
2	chr5:36786000-36789600	Enhancers	Stomach Mucosa	stomach
3	chr5:36786000-36790000	Enhancers	Fetal Intestine Small	intestine
4	chr5:36786600-36789800	Enhancers	Liver	Liver
5	chr5:36786600-36789800	Enhancers	HepG2	liver
6	chr5:36787800-36788600	Weak transcription	Fetal Intestine Large	intestine

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