Variant report

Variant	rs16844658
Chromosome Location	chr1:172482111-172482112
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]
rs10489279	0.85[LWK][hapmap]
rs3021328	1.00[GIH][hapmap]
rs5014423	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6672570	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]
rs73032168	0.98[AFR][1000 genomes]
rs73032170	0.97[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172480400-172483000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr1:172480800-172487800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr1:172481600-172482400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr1:172481600-172482400	Enhancers	Monocytes-CD14+_RO01746	blood

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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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