Variant report

Variant	rs9863891
Chromosome Location	chr3:140766012-140766013
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11708480	0.99[ASN][1000 genomes]
rs2114514	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4683541	0.90[ASN][1000 genomes]
rs6810025	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs919154	0.91[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs9826671	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432488	chr3:140752302-140790302	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140764800-140769400	Weak transcription	Right Atrium	heart
2	chr3:140765400-140767000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:140765800-140766600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr3:140765800-140766600	Enhancers	NHEK	skin
5	chr3:140765800-140766800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr3:140766000-140766600	Enhancers	HMEC	breast

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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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