Variant report

Variant	rs7525662
Chromosome Location	chr1:73533199-73533200
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10889999	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11210099	0.84[ASN][1000 genomes]
rs11210100	0.84[ASN][1000 genomes]
rs11210103	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11210107	0.94[ASN][1000 genomes]
rs11210114	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11210115	0.83[EUR][1000 genomes]
rs11210117	0.83[EUR][1000 genomes]
rs11210118	0.83[EUR][1000 genomes]
rs11210119	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11210120	0.83[EUR][1000 genomes]
rs11210127	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11803263	0.85[ASN][1000 genomes]
rs12025473	0.87[ASN][1000 genomes]
rs12033354	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12042865	0.83[ASN][1000 genomes]
rs12044276	0.91[ASN][1000 genomes]
rs12122055	0.81[EUR][1000 genomes]
rs12122377	0.88[ASN][1000 genomes]
rs12567284	0.94[ASN][1000 genomes]
rs12724536	0.91[ASN][1000 genomes]
rs12729632	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12748124	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs36093886	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4233093	0.87[ASN][1000 genomes]
rs4430278	0.80[ASN][1000 genomes]
rs4477222	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4559446	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4579707	0.86[ASN][1000 genomes]
rs4589057	0.88[ASN][1000 genomes]
rs4622012	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4649975	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4649976	0.83[EUR][1000 genomes]
rs6424507	0.86[ASN][1000 genomes]
rs6424508	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6657069	0.82[ASN][1000 genomes]
rs6667006	0.86[ASN][1000 genomes]
rs6667756	0.88[ASN][1000 genomes]
rs66820357	0.91[ASN][1000 genomes]
rs6693460	0.97[ASN][1000 genomes]
rs6696689	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7516446	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7516673	0.84[ASN][1000 genomes]
rs7519995	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7526372	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7528197	0.83[EUR][1000 genomes]
rs7528312	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7528791	0.87[ASN][1000 genomes]
rs7536364	0.86[ASN][1000 genomes]
rs7540420	0.89[ASN][1000 genomes]
rs7552256	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7554291	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9919151	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9970090	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	nsv1012319	chr1:73337418-73547086	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546568	chr1:73529275-73556846	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:73531000-73533600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr1:73531000-73534000	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:73531400-73533600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr1:73531800-73533600	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links