Variant report

Variant	rs16866901
Chromosome Location	chr2:180532226-180532227
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16866891	0.97[AFR][1000 genomes]
rs16866893	0.97[AFR][1000 genomes]
rs16866916	1.00[AFR][1000 genomes]
rs16866918	0.97[AFR][1000 genomes]
rs55935953	0.81[AFR][1000 genomes]
rs58946184	1.00[AFR][1000 genomes]
rs59659952	0.82[AFR][1000 genomes]
rs73976035	0.97[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv961361	chr2:180530964-180534513	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180531800-180536400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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