Variant report

Variant	rs72811739
Chromosome Location	chr2:56177394-56177395
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs3791678	1.00[AMR][1000 genomes]
rs55818621	1.00[AMR][1000 genomes]
rs55832400	1.00[AMR][1000 genomes]
rs59265286	1.00[AMR][1000 genomes]
rs72805677	1.00[AMR][1000 genomes]
rs72807753	1.00[AMR][1000 genomes]
rs72807766	1.00[AMR][1000 genomes]
rs72807767	1.00[AMR][1000 genomes]
rs72807770	1.00[AMR][1000 genomes]
rs72807773	1.00[AMR][1000 genomes]
rs72807774	1.00[AMR][1000 genomes]
rs72807775	1.00[AMR][1000 genomes]
rs72811708	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72811720	1.00[AMR][1000 genomes]
rs72811729	1.00[AMR][1000 genomes];0.92[EUR][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	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv874161	chr2:56154316-56203798	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56171000-56185000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:56175600-56181400	Weak transcription	HUVEC	blood vessel
3	chr2:56176000-56181400	Weak transcription	Adipose Nuclei	Adipose
4	chr2:56176400-56177400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:56176400-56181000	Weak transcription	Osteobl	bone
6	chr2:56176400-56181400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:56176600-56181200	Weak transcription	Fetal Kidney	kidney
8	chr2:56176800-56177800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:56177000-56181400	Weak transcription	Hela-S3	cervix

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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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