Variant report

Variant	rs67830346
Chromosome Location	chr2:209413255-209413256
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs55920681	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58341306	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59761715	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60524525	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs66478682	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66552766	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66682063	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67484901	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs68066160	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7566907	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7567228	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7579346	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209407800-209414400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:209410600-209414200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr2:209411200-209414000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr2:209411400-209413600	Weak transcription	K562	blood
5	chr2:209412800-209413400	Enhancers	Small Intestine	intestine
6	chr2:209413200-209414000	Enhancers	Fetal Heart	heart
7	chr2:209413200-209414200	Enhancers	Placenta	Placenta

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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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