Variant report

Variant	rs7525086
Chromosome Location	chr1:211897587-211897588
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11119797	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12123627	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12130915	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12145195	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12145981	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56230302	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7512315	0.89[EUR][1000 genomes]
rs7543710	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7545954	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211879200-211913600	Weak transcription	Right Atrium	heart
2	chr1:211895400-211897600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr1:211896400-211909000	Weak transcription	Fetal Intestine Small	intestine
4	chr1:211896600-211897600	Enhancers	K562	blood
5	chr1:211896600-211898800	Enhancers	Pancreas	Pancrea
6	chr1:211896600-211898800	Enhancers	Spleen	Spleen
7	chr1:211897000-211898400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:211897200-211897600	Weak transcription	Ovary	ovary
9	chr1:211897200-211899200	Enhancers	HepG2	liver

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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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