Variant report

Variant	rs586773
Chromosome Location	chr11:73696610-73696611
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs3019463	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34408426	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs591758	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs599277	0.88[ASN][1000 genomes]
rs603950	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs605442	0.82[ASN][1000 genomes]
rs621976	1.00[ASN][1000 genomes]
rs632862	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs653529	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs655717	0.88[ASN][1000 genomes]
rs659366	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs660339	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs673494	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs675547	0.99[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	nsv492091	chr11:73285970-73844424	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs586773	UCP2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73695200-73696800	Enhancers	GM12878-XiMat	blood
2	chr11:73695200-73702400	Weak transcription	Right Atrium	heart
3	chr11:73695200-73711000	Weak transcription	Fetal Intestine Small	intestine
4	chr11:73695400-73697000	Weak transcription	Spleen	Spleen
5	chr11:73695600-73696800	Enhancers	Primary T cells from cord blood	blood
6	chr11:73696000-73697600	Weak transcription	Primary B cells from peripheral blood	blood
7	chr11:73696000-73699200	Weak transcription	HepG2	liver
8	chr11:73696000-73701000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:73696000-73701400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr11:73696000-73701600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:73696000-73701600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr11:73696000-73701800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr11:73696000-73701800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr11:73696000-73702200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr11:73696200-73697200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr11:73696200-73697800	Weak transcription	Primary B cells from cord blood	blood
17	chr11:73696400-73696800	Weak transcription	K562	blood

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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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