Variant report

Variant	rs73405684
Chromosome Location	chr7:103625627-103625628
allele	A/G
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]
rs73405688	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73405690	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73405692	0.88[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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103613800-103627800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:103624400-103625800	Weak transcription	K562	blood
3	chr7:103625600-103626600	Flanking Active TSS	HepG2	liver

Quick Search:

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

what's new

Quick links