Variant report

Variant	rs56807379
Chromosome Location	chr2:31286392-31286393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17010623	1.00[EUR][1000 genomes]
rs60000683	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6726827	1.00[EUR][1000 genomes]
rs72854822	1.00[EUR][1000 genomes]
rs72854824	1.00[EUR][1000 genomes]
rs72854829	1.00[EUR][1000 genomes]
rs72854834	1.00[EUR][1000 genomes]
rs72854839	1.00[EUR][1000 genomes]
rs72854851	1.00[EUR][1000 genomes]
rs72854856	1.00[EUR][1000 genomes]
rs72854858	0.83[AMR][1000 genomes]
rs73923381	1.00[EUR][1000 genomes]
rs7575804	0.83[AMR][1000 genomes]
rs9308915	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	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31278200-31293000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:31278200-31310800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:31278800-31306800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr2:31281000-31290000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:31283200-31292200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:31283800-31286600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr2:31284000-31301800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr2:31284200-31288400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:31284600-31288800	Weak transcription	Fetal Kidney	kidney
10	chr2:31286000-31289800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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