Variant report

Variant	rs72777081
Chromosome Location	chr5:91745264-91745265
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10041056	1.00[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs10041199	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10052520	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10055515	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10055632	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10057380	0.96[AFR][1000 genomes]
rs10063190	0.96[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs10065964	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10073874	0.91[EUR][1000 genomes]
rs13354246	0.96[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs72777068	0.91[EUR][1000 genomes]
rs72777069	0.91[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91744400-91745400	Enhancers	NHDF-Ad	bronchial
2	chr5:91744800-91745800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:91745000-91745800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr5:91745000-91745800	Enhancers	Fetal Heart	heart
5	chr5:91745200-91745600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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