Variant report

Variant	rs4576248
Chromosome Location	chr6:55493803-55493804
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2065028	1.00[EUR][1000 genomes]
rs55778645	1.00[AMR][1000 genomes]
rs56750083	1.00[AMR][1000 genomes]
rs57385665	1.00[AMR][1000 genomes]
rs58284917	1.00[AMR][1000 genomes]
rs59347412	1.00[AMR][1000 genomes]
rs60070969	1.00[AMR][1000 genomes]
rs6909150	1.00[AMR][1000 genomes]
rs6928231	1.00[MEX][hapmap]
rs6932083	1.00[AMR][1000 genomes]
rs73446194	1.00[AMR][1000 genomes]
rs73744903	1.00[AMR][1000 genomes]
rs73744908	1.00[AMR][1000 genomes]
rs7766232	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7767545	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1026411	chr6:55372845-55653498	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3474008	chr6:55491689-55494295	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	esv3474009	chr6:55491689-55494295	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3393454	chr6:55491818-55494366	Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv3429791	chr6:55491968-55494116	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55479400-55504000	Weak transcription	Pancreatic Islets	Pancreatic Islet

Quick Search:

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

what's new

Quick links