Variant report

Variant	rs267291
Chromosome Location	chr5:114635340-114635341
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1005056	1.00[ASW][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap]
rs12657293	0.88[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs169127	0.83[CHB][hapmap];0.84[AMR][1000 genomes]
rs2112362	0.86[CHB][hapmap]
rs2605182	1.00[YRI][hapmap]
rs267293	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs267296	1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2909841	0.82[CHB][hapmap]
rs3095906	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4705731	1.00[MEX][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114632200-114641800	Weak transcription	Stomach Mucosa	stomach

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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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