Variant report

Variant	rs10166144
Chromosome Location	chr2:21453733-21453734
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10170323	0.94[EUR][1000 genomes]
rs10177017	0.82[EUR][1000 genomes]
rs10183198	0.94[EUR][1000 genomes]
rs10198972	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs13387827	0.94[EUR][1000 genomes]
rs13398007	0.94[EUR][1000 genomes]
rs312029	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67144154	0.80[AMR][1000 genomes];0.84[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	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21449000-21454800	Weak transcription	Spleen	Spleen
2	chr2:21451600-21461800	Weak transcription	Aorta	Aorta
3	chr2:21452400-21457600	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:21453400-21454800	Weak transcription	K562	blood

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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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