Variant report

Variant	rs56292592
Chromosome Location	chr2:10993751-10993752
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs73915848	1.00[AFR][1000 genomes]
rs73915850	1.00[AFR][1000 genomes]
rs73915851	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	nsv818988	chr2:10990198-11009610	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10979400-11000400	Weak transcription	Fetal Brain Male	brain
2	chr2:10988800-10993800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:10989200-11003200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:10989800-10996800	Weak transcription	Right Atrium	heart
5	chr2:10993600-10994200	Enhancers	Left Ventricle	heart
6	chr2:10993600-10995000	Enhancers	Right Ventricle	heart

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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

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