Variant report

Variant	rs506284
Chromosome Location	chr3:23048922-23048923
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs520582	0.87[EUR][1000 genomes]
rs528649	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs529219	0.83[CEU][hapmap];0.87[EUR][1000 genomes]
rs535689	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs537660	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs549968	0.87[CEU][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55652823	0.89[EUR][1000 genomes]
rs601598	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs621200	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs633464	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs711725	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs822768	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs822775	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs843989	0.80[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23045200-23052200	Weak transcription	Fetal Heart	heart
2	chr3:23047200-23049200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:23047400-23049000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr3:23047400-23049200	Weak transcription	NHEK	skin
5	chr3:23047400-23049600	Weak transcription	HMEC	breast
6	chr3:23048600-23049400	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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