Variant report

Variant	rs7643926
Chromosome Location	chr3:24707093-24707094
allele	C/T
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:16)

rs_ID	r²[population]
rs11928551	0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs12106829	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17787397	0.86[ASN][1000 genomes]
rs2362754	0.81[ASN][1000 genomes]
rs4544557	0.85[ASN][1000 genomes]
rs6550887	0.88[ASN][1000 genomes]
rs6762059	0.86[ASN][1000 genomes]
rs6767967	0.85[ASN][1000 genomes]
rs6770162	0.83[ASN][1000 genomes]
rs6771221	0.91[ASN][1000 genomes]
rs6777417	0.86[ASN][1000 genomes]
rs7644196	0.86[ASN][1000 genomes]
rs9811110	0.85[ASN][1000 genomes]
rs9812637	0.95[CHB][hapmap];0.94[CHD][hapmap];0.88[JPT][hapmap];0.80[TSI][hapmap];0.90[ASN][1000 genomes]
rs9817530	0.87[CHD][hapmap];0.88[JPT][hapmap];0.80[TSI][hapmap]
rs9843745	0.88[CHD][hapmap];0.88[JPT][hapmap];0.83[TSI][hapmap]

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	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	nsv1005314	chr3:24690692-24813960	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv589950	chr3:24694021-24816974	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24704200-24726000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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