Variant report

Variant	rs28425539
Chromosome Location	chr6:25755101-25755102
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10046149	1.00[AMR][1000 genomes]
rs10223505	1.00[AMR][1000 genomes]
rs9461193	1.00[AMR][1000 genomes]
rs9461194	1.00[AMR][1000 genomes]
rs9461208	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9461213	1.00[AMR][1000 genomes]
rs9467533	1.00[AMR][1000 genomes]
rs9467540	1.00[AMR][1000 genomes]
rs9467553	1.00[AMR][1000 genomes]
rs9467554	1.00[AMR][1000 genomes]
rs9467557	1.00[AMR][1000 genomes]
rs9467559	1.00[AMR][1000 genomes]
rs9467563	1.00[AMR][1000 genomes]
rs9467564	1.00[AMR][1000 genomes]
rs9467567	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9467597	1.00[AMR][1000 genomes]
rs9467605	1.00[AMR][1000 genomes]
rs9467611	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv427747	chr6:25641380-25908218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv969355	chr6:25733459-25779530	Genic enhancers Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25753400-25756600	Enhancers	HepG2	liver
2	chr6:25754600-25760000	Active TSS	Rectal Mucosa Donor 29	rectum
3	chr6:25754800-25755200	Flanking Active TSS	Liver	Liver
4	chr6:25754800-25755600	Active TSS	Rectal Mucosa Donor 31	rectum
5	chr6:25754800-25756000	Active TSS	Fetal Intestine Small	intestine
6	chr6:25754800-25756200	Active TSS	Fetal Intestine Large	intestine
7	chr6:25754800-25757000	Active TSS	Duodenum Mucosa	Duodenum
8	chr6:25755000-25755200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr6:25755000-25756800	Active TSS	Colonic Mucosa	Colon
10	chr6:25755000-25756800	Active TSS	Pancreas	Pancrea
11	chr6:25755000-25756800	Active TSS	Rectal Smooth Muscle	rectum

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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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