Variant report

Variant	rs12523537
Chromosome Location	chr5:42373683-42373684
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	chr5:42370907..42372657-chr5:42372829..42374806,2	K562	blood:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10064323	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10941576	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1117110	0.91[ASN][1000 genomes]
rs11738365	0.91[ASN][1000 genomes]
rs12513643	0.98[ASN][1000 genomes]
rs12515480	0.87[ASN][1000 genomes]
rs12517368	0.87[ASN][1000 genomes]
rs12517931	0.98[ASN][1000 genomes]
rs12518010	0.89[ASN][1000 genomes]
rs12518274	0.87[ASN][1000 genomes]
rs12520318	0.98[ASN][1000 genomes]
rs12522222	0.89[ASN][1000 genomes]
rs12522421	0.89[ASN][1000 genomes]
rs12654242	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13185872	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1396768	0.91[ASN][1000 genomes]
rs1396775	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1472947	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1509455	0.91[ASN][1000 genomes]
rs1509456	0.91[ASN][1000 genomes]
rs1509460	0.93[ASN][1000 genomes]
rs1605851	0.88[ASN][1000 genomes]
rs16872537	0.94[ASN][1000 genomes]
rs16872543	0.94[ASN][1000 genomes]
rs16872564	0.89[ASN][1000 genomes]
rs1858136	0.91[ASN][1000 genomes]
rs1858138	0.98[ASN][1000 genomes]
rs1876790	0.96[ASN][1000 genomes]
rs1960498	0.91[ASN][1000 genomes]
rs1979994	0.89[ASN][1000 genomes]
rs2036745	0.89[ASN][1000 genomes]
rs2202883	0.91[ASN][1000 genomes]
rs2221712	0.91[ASN][1000 genomes]
rs2395970	0.91[ASN][1000 genomes]
rs28498583	0.89[ASN][1000 genomes]
rs28943877	0.94[ASN][1000 genomes]
rs2940912	0.93[ASN][1000 genomes]
rs2940914	0.91[ASN][1000 genomes]
rs2940917	0.89[ASN][1000 genomes]
rs2940918	0.83[ASN][1000 genomes]
rs2940919	0.89[ASN][1000 genomes]
rs2940922	0.89[ASN][1000 genomes]
rs2940923	0.91[ASN][1000 genomes]
rs2940927	0.98[ASN][1000 genomes]
rs2940934	0.91[ASN][1000 genomes]
rs2940940	0.98[ASN][1000 genomes]
rs2940945	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2972394	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972406	0.91[ASN][1000 genomes]
rs2972407	0.91[ASN][1000 genomes]
rs2972408	0.91[ASN][1000 genomes]
rs2972410	0.89[ASN][1000 genomes]
rs2972411	0.89[ASN][1000 genomes]
rs2972412	0.89[ASN][1000 genomes]
rs2972413	0.89[ASN][1000 genomes]
rs3764453	0.96[ASN][1000 genomes]
rs4358532	0.95[ASN][1000 genomes]
rs4866781	0.89[ASN][1000 genomes]
rs4866782	0.89[ASN][1000 genomes]
rs4866788	0.85[ASN][1000 genomes]
rs4866795	0.94[ASN][1000 genomes]
rs4866896	0.94[ASN][1000 genomes]
rs4866901	0.94[ASN][1000 genomes]
rs4866919	0.89[ASN][1000 genomes]
rs906817	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9686537	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9687863	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs979233	1.00[ASN][1000 genomes]
rs991592	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
2	nsv492147	chr5:41902086-42896162	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
3	nsv880518	chr5:42231896-42375243	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv881375	chr5:42254097-42442715	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv948514	chr5:42270161-42519262	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42373600-42373800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:42373600-42374200	Enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links