Variant report

Variant	rs2455250
Chromosome Location	chr5:36479375-36479376
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12054904	1.00[JPT][hapmap]
rs16903085	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2455247	1.00[ASN][1000 genomes]
rs2455248	1.00[ASN][1000 genomes]
rs2455249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2455253	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs2455254	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs2468501	1.00[ASN][1000 genomes]
rs2468531	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6868930	1.00[ASN][1000 genomes]
rs6885914	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36478800-36479800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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