Variant report

Variant	rs10450737
Chromosome Location	chr12:105909277-105909278
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10450736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861437	0.80[AFR][1000 genomes]
rs10861440	0.80[AFR][1000 genomes]
rs10861445	0.80[AFR][1000 genomes]
rs10861446	0.80[AFR][1000 genomes]
rs10861451	0.80[AFR][1000 genomes]
rs10861452	0.80[AFR][1000 genomes]
rs11112563	0.80[AFR][1000 genomes]
rs11112564	0.80[AFR][1000 genomes]
rs11112565	0.80[AFR][1000 genomes]
rs11112570	0.80[AFR][1000 genomes]
rs11513895	0.85[AFR][1000 genomes]
rs12305323	0.80[AFR][1000 genomes]
rs12371780	0.80[AFR][1000 genomes]
rs17037274	0.80[AFR][1000 genomes]
rs73387413	0.80[AFR][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	nsv899501	chr12:105819046-105950801	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv832507	chr12:105821685-106005186	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 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	chr12:105906200-105913200	Weak transcription	HUVEC	blood vessel

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

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