Variant report

Variant	rs7652529
Chromosome Location	chr3:54468033-54468034
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs13327362	0.82[EUR][1000 genomes]
rs1868500	0.82[EUR][1000 genomes]
rs1992964	0.96[ASN][1000 genomes]
rs4131315	0.90[ASN][1000 genomes]
rs4974369	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6445660	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6768189	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73089420	0.96[ASN][1000 genomes]
rs73089428	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73089448	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73089451	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7428295	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7429237	0.91[ASN][1000 genomes]
rs7615599	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9855860	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9861155	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9882285	0.96[ASN][1000 genomes]
rs9882299	0.96[ASN][1000 genomes]
rs9882553	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv817210	chr3:54365684-54511164	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv428084	chr3:54404258-54742756	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1010348	chr3:54435563-54508115	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv876807	chr3:54453655-54501086	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv998970	chr3:54455794-54516789	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv876808	chr3:54459688-54501086	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv876809	chr3:54459688-54501086	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:54463000-54469200	Weak transcription	Hela-S3	cervix
2	chr3:54463600-54469000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:54463600-54469000	Weak transcription	NHDF-Ad	bronchial
4	chr3:54467600-54468400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr3:54467600-54468400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:54467600-54468400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:54467600-54468400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:54467600-54468600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:54467800-54468400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:54467800-54469200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:54468000-54468400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:54468000-54473000	Weak transcription	Gastric	stomach

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