Variant report

Variant	rs10145436
Chromosome Location	chr14:84505181-84505182
allele	A/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:8)

rs_ID	r²[population]
rs10134358	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs17119559	0.94[AFR][1000 genomes]
rs58445096	0.82[AFR][1000 genomes]
rs6574768	0.87[AFR][1000 genomes]
rs7140689	0.87[AFR][1000 genomes]
rs7142486	0.86[AFR][1000 genomes]
rs7142519	0.86[AFR][1000 genomes]
rs7161645	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84504200-84507600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:84504200-84508200	Weak transcription	Fetal Heart	heart

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