Variant report

Variant	rs16902021
Chromosome Location	chr5:35431463-35431464
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16902024	1.00[ASW][hapmap];0.92[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6867993	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6881409	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6888863	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73747430	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs73747431	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35430200-35431800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr5:35430400-35431800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr5:35431000-35431800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr5:35431200-35431600	Enhancers	Placenta Amnion	Placenta Amnion
5	chr5:35431400-35431600	Enhancers	Placenta	Placenta

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