Variant report

Variant	rs9530881
Chromosome Location	chr13:79845908-79845909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs12427538	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12428306	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9530882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9545027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9545045	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9545088	1.00[LWK][hapmap]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:79843600-79846000	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr13:79843600-79846200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:79843600-79846200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr13:79844600-79846200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr13:79844800-79846000	Enhancers	HepG2	liver
6	chr13:79845200-79846200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:79845800-79846000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr13:79845800-79846000	Enhancers	H9 Derived Neuron 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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