Variant report

Variant	rs4943450
Chromosome Location	chr13:37751878-37751879
allele	A/G
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]
rs1199994	0.81[EUR][1000 genomes]
rs1537946	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17055019	0.93[ASN][1000 genomes]
rs2323397	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4509889	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4943449	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58001767	0.87[ASN][1000 genomes]
rs6563513	0.97[ASN][1000 genomes]
rs6563516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8001995	0.97[ASN][1000 genomes]
rs938215	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs945633	0.93[ASN][1000 genomes]
rs9532007	0.97[ASN][1000 genomes]
rs9576193	0.93[ASN][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	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37747400-37752400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr13:37747600-37752400	Enhancers	Fetal Lung	lung
3	chr13:37750000-37752200	Enhancers	Colon Smooth Muscle	Colon
4	chr13:37751000-37752000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr13:37751000-37752000	Weak transcription	NHLF	lung
6	chr13:37751400-37752000	Weak transcription	NHDF-Ad	bronchial
7	chr13:37751800-37766000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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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