Variant report

Variant	rs10426988
Chromosome Location	chr19:45329130-45329131
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10402103	1.00[AFR][1000 genomes]
rs10404441	1.00[AFR][1000 genomes]
rs10410517	0.89[AFR][1000 genomes]
rs10415477	1.00[AFR][1000 genomes]
rs28399632	1.00[AFR][1000 genomes]
rs28528835	0.89[AFR][1000 genomes]
rs9967601	0.89[AFR][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	esv3332339	chr19:45321161-45351386	Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45326800-45331800	Weak transcription	Liver	Liver
2	chr19:45326800-45331800	Weak transcription	Right Atrium	heart
3	chr19:45329000-45329200	Enhancers	Right Ventricle	heart

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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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