Variant report

Variant	rs57034259
Chromosome Location	chr1:219942104-219942105
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11803657	0.98[EUR][1000 genomes]
rs11805110	0.96[EUR][1000 genomes]
rs11805132	0.98[EUR][1000 genomes]
rs11808330	0.98[EUR][1000 genomes]
rs12067347	0.98[EUR][1000 genomes]
rs12072368	0.98[EUR][1000 genomes]
rs12077018	0.96[EUR][1000 genomes]
rs13375416	0.98[EUR][1000 genomes]
rs17006699	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17551627	0.82[AMR][1000 genomes]
rs2066418	0.90[EUR][1000 genomes]
rs2378324	0.98[EUR][1000 genomes]
rs4308987	0.90[EUR][1000 genomes]
rs55646081	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55712001	0.98[EUR][1000 genomes]
rs55753922	0.98[EUR][1000 genomes]
rs55800251	0.98[EUR][1000 genomes]
rs55828554	0.98[EUR][1000 genomes]
rs55882931	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55920559	0.98[EUR][1000 genomes]
rs55931064	0.98[EUR][1000 genomes]
rs55956414	0.98[EUR][1000 genomes]
rs55977511	0.98[EUR][1000 genomes]
rs55981027	0.98[EUR][1000 genomes]
rs56073293	0.98[EUR][1000 genomes]
rs56105497	0.98[EUR][1000 genomes]
rs56170642	0.98[EUR][1000 genomes]
rs56213832	0.98[EUR][1000 genomes]
rs56286098	0.98[EUR][1000 genomes]
rs56331091	0.98[EUR][1000 genomes]
rs58859585	0.98[EUR][1000 genomes]
rs60659404	0.98[EUR][1000 genomes]
rs60827853	0.98[EUR][1000 genomes]
rs6676773	0.98[EUR][1000 genomes]
rs6690503	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6692539	0.98[EUR][1000 genomes]
rs72738726	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72738731	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72738733	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72738744	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72738745	0.98[EUR][1000 genomes]
rs72738747	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72738748	0.98[EUR][1000 genomes]
rs72738750	0.98[EUR][1000 genomes]
rs72738751	0.98[EUR][1000 genomes]
rs72738753	0.98[EUR][1000 genomes]
rs72738758	0.98[EUR][1000 genomes]
rs72738763	0.98[EUR][1000 genomes]
rs72738765	0.98[EUR][1000 genomes]
rs72738768	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72738769	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72738771	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72738772	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7533484	0.98[EUR][1000 genomes]
rs7535102	0.98[EUR][1000 genomes]
rs7535834	0.98[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006393	chr1:219925261-220126458	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:219940400-219944000	Weak transcription	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links