Variant report

Variant	rs8009490
Chromosome Location	chr14:39686584-39686585
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10136285	0.95[ASN][1000 genomes]
rs10136309	0.95[ASN][1000 genomes]
rs10138869	0.94[ASN][1000 genomes]
rs6571906	0.93[ASN][1000 genomes]
rs7140164	0.97[ASN][1000 genomes]
rs7143393	0.95[ASN][1000 genomes]
rs7145048	0.91[ASN][1000 genomes]
rs7145343	0.93[ASN][1000 genomes]
rs7145345	0.93[ASN][1000 genomes]
rs7146289	0.93[ASN][1000 genomes]
rs7157271	0.94[ASN][1000 genomes]
rs7160180	0.95[ASN][1000 genomes]
rs74048717	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1246	chr14:39656597-39701520	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1053133	chr14:39657535-39770729	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv977460	chr14:39684663-39690168	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39674000-39705400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:39681600-39686600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr14:39685200-39687400	Enhancers	Hela-S3	cervix
4	chr14:39686400-39686600	Enhancers	K562	blood
5	chr14:39686400-39687000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr14:39686400-39687200	Enhancers	A549	lung
7	chr14:39686400-39687400	Enhancers	HepG2	liver
8	chr14:39686400-39688400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:39686400-39688600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr14:39686400-39688600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:39686400-39688600	Enhancers	Small Intestine	intestine
12	chr14:39686400-39688600	Enhancers	HMEC	breast
13	chr14:39686400-39688600	Enhancers	NHEK	skin
14	chr14:39686400-39688800	Enhancers	HUVEC	blood vessel

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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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