Variant report

Variant	rs16902024
Chromosome Location	chr5:35431679-35431680
allele	C/T
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]
rs16902021	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:4 , 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	chr5:35431600-35436600	Weak transcription	Placenta Amnion	Placenta Amnion

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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

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