Variant report

Variant	rs12537578
Chromosome Location	chr7:103637033-103637034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10953400	0.97[AFR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12533473	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17157903	0.88[CHB][hapmap];0.89[ASN][1000 genomes]
rs35898997	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58041247	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58095345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103636200-103637400	Flanking Active TSS	K562	blood
2	chr7:103636600-103638000	Enhancers	Liver	Liver
3	chr7:103636600-103638000	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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