Variant report

Variant	rs4693021
Chromosome Location	chr4:81309456-81309457
allele	A/C
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]
rs1039051	0.86[AFR][1000 genomes]
rs12642262	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1495483	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1495485	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1495488	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2007145	0.83[AMR][1000 genomes]
rs4693100	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4693384	0.83[AMR][1000 genomes]
rs4693688	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6534890	0.83[AMR][1000 genomes]
rs6826195	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6849232	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81291000-81310200	Weak transcription	Osteobl	bone
2	chr4:81308200-81314800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:81308600-81314600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:81309200-81309600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:81309400-81310000	Weak transcription	iPS DF 19.11 Cell Line	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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