Variant report

Variant	rs74126521
Chromosome Location	chr10:25583127-25583128
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10508692	0.85[ASN][1000 genomes]
rs1413400	0.91[ASN][1000 genomes]
rs1416993	0.91[ASN][1000 genomes]
rs1416994	0.91[ASN][1000 genomes]
rs16925561	0.93[ASN][1000 genomes]
rs55801305	0.91[ASN][1000 genomes]
rs56084254	0.89[ASN][1000 genomes]
rs56257605	0.89[ASN][1000 genomes]
rs58585465	0.91[ASN][1000 genomes]
rs58942965	0.91[ASN][1000 genomes]
rs58968345	0.94[ASN][1000 genomes]
rs59521850	0.91[ASN][1000 genomes]
rs60268096	0.91[ASN][1000 genomes]
rs60352386	0.88[ASN][1000 genomes]
rs60876342	0.94[ASN][1000 genomes]
rs61082972	0.91[ASN][1000 genomes]
rs61105987	0.89[ASN][1000 genomes]
rs61108946	0.91[ASN][1000 genomes]
rs61271645	0.94[ASN][1000 genomes]
rs61530525	0.91[ASN][1000 genomes]
rs66463292	0.91[ASN][1000 genomes]
rs66539540	0.91[ASN][1000 genomes]
rs66810403	0.91[ASN][1000 genomes]
rs66924755	0.89[ASN][1000 genomes]
rs66963587	0.91[ASN][1000 genomes]
rs67069034	0.91[ASN][1000 genomes]
rs67389824	0.91[ASN][1000 genomes]
rs67675896	0.91[ASN][1000 genomes]
rs67709672	0.91[ASN][1000 genomes]
rs67733590	0.91[ASN][1000 genomes]
rs67963266	0.89[ASN][1000 genomes]
rs67969515	0.89[ASN][1000 genomes]
rs68159928	0.91[ASN][1000 genomes]
rs7093650	0.91[ASN][1000 genomes]
rs7093651	0.91[ASN][1000 genomes]
rs7093692	0.91[ASN][1000 genomes]
rs72792092	0.91[ASN][1000 genomes]
rs72794261	0.85[ASN][1000 genomes]
rs73608266	0.91[ASN][1000 genomes]
rs73608267	0.85[ASN][1000 genomes]
rs74123863	0.93[ASN][1000 genomes]
rs7476751	0.91[ASN][1000 genomes]
rs7904501	0.91[ASN][1000 genomes]
rs9663151	0.94[ASN][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	esv2761583	chr10:25525657-25722444	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr10:25582000-25592000	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr10:25582200-25583400	Weak transcription	A549	lung

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links