Variant report

Variant	rs73405688
Chromosome Location	chr7:103628391-103628392
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10216187	0.83[EUR][1000 genomes]
rs10216198	0.83[EUR][1000 genomes]
rs10273035	0.83[EUR][1000 genomes]
rs10487182	0.83[EUR][1000 genomes]
rs11971265	0.83[EUR][1000 genomes]
rs11972170	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17158144	0.83[EUR][1000 genomes]
rs17158288	0.83[EUR][1000 genomes]
rs55825925	0.83[EUR][1000 genomes]
rs56334899	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60375583	0.83[EUR][1000 genomes]
rs73405684	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73405690	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73405692	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73409925	0.83[EUR][1000 genomes]
rs73409927	0.83[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103626600-103629000	Active TSS	HepG2	liver
2	chr7:103628000-103628400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:103628000-103628600	Flanking Active TSS	K562	blood
4	chr7:103628200-103629000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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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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