Variant report

Variant	rs62182997
Chromosome Location	chr2:212603051-212603052
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs62182966	1.00[EUR][1000 genomes]
rs62182967	1.00[EUR][1000 genomes]
rs62182979	1.00[EUR][1000 genomes]
rs62182982	1.00[EUR][1000 genomes]
rs62182983	1.00[EUR][1000 genomes]
rs62182987	1.00[EUR][1000 genomes]
rs62182990	1.00[EUR][1000 genomes]
rs62182995	1.00[EUR][1000 genomes]
rs62182998	1.00[AFR][1000 genomes]
rs62183022	1.00[EUR][1000 genomes]
rs62183025	1.00[EUR][1000 genomes]
rs62183027	1.00[EUR][1000 genomes]
rs62184484	1.00[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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 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	chr2:212602400-212606200	Weak transcription	Fetal Heart	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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