Variant report

Variant	rs538719
Chromosome Location	chr6:145595964-145595965
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs483603	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs497174	0.99[ASN][1000 genomes]
rs505814	0.91[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs511290	0.95[ASN][1000 genomes]
rs529364	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs543638	0.84[ASN][1000 genomes]
rs545242	0.95[ASN][1000 genomes]
rs555720	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs557732	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs557970	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs566661	0.84[ASN][1000 genomes]
rs576429	0.95[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	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1022965	chr6:145374851-145635385	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145592600-145597200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:145593000-145599000	Weak transcription	Colon Smooth Muscle	Colon
3	chr6:145594600-145597200	Enhancers	Liver	Liver
4	chr6:145595600-145600200	Enhancers	HepG2	liver

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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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