Variant report

Variant	rs10124833
Chromosome Location	chr9:104039252-104039253
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10116399	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10118704	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10120191	1.00[ASN][1000 genomes]
rs10122456	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10122687	0.93[AFR][1000 genomes]
rs10124153	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12000705	0.94[AFR][1000 genomes]
rs12000720	0.91[AFR][1000 genomes]
rs13289265	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56065216	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6479047	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104032400-104040800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:104032400-104042000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:104038200-104054000	Weak transcription	Fetal Brain Male	brain
4	chr9:104039200-104050000	Weak transcription	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