Variant report

Variant	rs6672570
Chromosome Location	chr1:172481206-172481207
allele	A/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]
rs10489279	0.81[LWK][hapmap]
rs16844658	1.00[ASW][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3021328	1.00[GIH][hapmap]
rs5014423	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032168	0.93[AFR][1000 genomes]
rs73032170	0.92[AFR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172479400-172481600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr1:172480400-172483000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr1:172480800-172487800	Enhancers	Primary neutrophils fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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