Variant report

Variant	rs58041247
Chromosome Location	chr7:103633266-103633267
allele	C/T
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	0.88[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs12533473	0.93[ASN][1000 genomes]
rs12537578	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17157903	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35898997	0.95[ASN][1000 genomes]
rs58095345	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103631600-103636200	Enhancers	K562	blood
2	chr7:103632800-103633800	Weak transcription	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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