Variant report

Variant	rs1450425
Chromosome Location	chr18:44109033-44109034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11082532	0.84[JPT][hapmap];0.80[YRI][hapmap]
rs12327030	0.90[ASN][1000 genomes]
rs12458442	0.82[ASN][1000 genomes]
rs1868712	0.90[ASN][1000 genomes]
rs1893566	0.88[ASW][hapmap];0.84[JPT][hapmap];0.80[YRI][hapmap]
rs4263029	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4890667	0.95[CHB][hapmap];0.93[CHD][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs4890669	0.90[ASN][1000 genomes]
rs59252058	0.92[ASN][1000 genomes]
rs7237393	0.85[ASN][1000 genomes]
rs988213	0.88[ASN][1000 genomes]
rs9951898	0.94[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44086000-44114400	Weak transcription	Spleen	Spleen
2	chr18:44093200-44118600	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr18:44093200-44120400	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr18:44094000-44126000	Weak transcription	Adipose Nuclei	Adipose
5	chr18:44104600-44112800	Weak transcription	Lung	lung
6	chr18:44108600-44119400	Strong transcription	Monocytes-CD14+_RO01746	blood

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