Variant report

Variant	rs6756653
Chromosome Location	chr2:184344937-184344938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10931081	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10931082	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12472874	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12478259	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12613271	0.82[AMR][1000 genomes]
rs12693344	0.82[AMR][1000 genomes]
rs13021228	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13035800	0.82[AMR][1000 genomes]
rs13422198	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13432447	0.82[AMR][1000 genomes]
rs1370647	0.81[AMR][1000 genomes]
rs1438015	0.80[AMR][1000 genomes]
rs1438016	0.81[AMR][1000 genomes]
rs1898581	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs35765385	0.82[AMR][1000 genomes]
rs6728174	0.84[AMR][1000 genomes]
rs6732408	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6732731	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6732771	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6747311	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6747547	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6750012	0.81[AMR][1000 genomes]
rs6756529	0.87[AFR][1000 genomes]
rs7567519	0.81[AMR][1000 genomes]
rs7567725	0.82[AMR][1000 genomes]
rs7567749	0.82[AMR][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	esv3416805	chr2:184342157-184345105	Enhancers Weak transcription	Chromatin interactive region	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	chr2:184342400-184352600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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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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