Variant report

Variant	rs2362767
Chromosome Location	chr3:24895707-24895708
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10865798	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12495571	0.85[ASN][1000 genomes]
rs12638345	1.00[ASN][1000 genomes]
rs1319984	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1994905	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1994906	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2362776	0.84[EUR][1000 genomes]
rs2362777	0.82[EUR][1000 genomes]
rs2885593	0.82[EUR][1000 genomes]
rs4858131	0.81[EUR][1000 genomes]
rs937262	0.92[ASN][1000 genomes]
rs9754535	0.81[EUR][1000 genomes]
rs9832148	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9864319	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9880358	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757862	chr3:24652513-24942926	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759135	chr3:24652513-24942926	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv834643	chr3:24779627-24942886	Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv3734	chr3:24861568-24906866	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1011730	chr3:24892941-24912030	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24888000-24897800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:24888000-24898000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr3:24892800-24897600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr3:24894800-24896200	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr3:24895400-24895800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:24895400-24896000	Enhancers	Fetal Kidney	kidney

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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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