Variant report

Variant	rs28404348
Chromosome Location	chr18:25189274-25189275
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1420941	1.00[AMR][1000 genomes]
rs1519131	1.00[AMR][1000 genomes]
rs16943888	1.00[AMR][1000 genomes]
rs1861781	1.00[AMR][1000 genomes]
rs2714375	1.00[AMR][1000 genomes]
rs3110549	1.00[AMR][1000 genomes]
rs3110550	1.00[AMR][1000 genomes]
rs56774619	1.00[AMR][1000 genomes]
rs7230612	1.00[AMR][1000 genomes]
rs7242276	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8083675	1.00[AMR][1000 genomes]
rs8094042	1.00[AMR][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	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr18:25185200-25195000	Weak transcription	H9 Cell Line	embryonic stem cell

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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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