Variant report

Variant	rs16943779
Chromosome Location	chr18:25163077-25163078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1420948	1.00[CHB][hapmap];1.00[AMR][1000 genomes]
rs1420952	1.00[CHB][hapmap];1.00[AMR][1000 genomes]
rs16943782	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16943789	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16943806	1.00[AMR][1000 genomes]
rs16943849	1.00[AMR][1000 genomes]
rs4800283	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4800816	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56387355	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57518255	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59085826	1.00[AMR][1000 genomes]
rs73412987	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73413000	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73414903	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73414911	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73414945	1.00[AMR][1000 genomes]
rs73944952	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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
2	nsv833602	chr18:24993030-25180823	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	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	chr18:25159000-25167400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr18:25159600-25163400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr18:25162000-25163200	ZNF genes & repeats	Fetal Intestine Small	intestine
4	chr18:25162600-25163600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr18:25162600-25168000	Enhancers	Fetal Intestine Large	intestine
6	chr18:25163000-25163600	Enhancers	Skeletal Muscle Female	skeletal muscle

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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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