Variant report

Variant	rs1513226
Chromosome Location	chr3:23070183-23070184
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11925573	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11929219	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12629336	1.00[AMR][1000 genomes]
rs56708904	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs73821126	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73821127	0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7641080	0.80[AFR][1000 genomes];0.84[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23068800-23071200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr3:23069400-23071200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr3:23069400-23071600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr3:23069400-23071600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr3:23070000-23070400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr3:23070000-23070400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr3:23070000-23070400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr3:23070000-23071600	Enhancers	iPS-20b 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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