Variant report

Variant	rs1021346
Chromosome Location	chr14:63251059-63251060
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]
rs11158452	0.83[ASN][1000 genomes]
rs12433281	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12882526	0.84[AFR][1000 genomes]
rs12891322	0.87[ASN][1000 genomes]
rs12891982	0.95[AFR][1000 genomes]
rs12893269	0.81[AFR][1000 genomes]
rs2171876	0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35679534	0.95[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs35872261	0.84[AFR][1000 genomes]
rs56397364	1.00[AFR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7493979	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs961066	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63249200-63252000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr14:63249200-63253000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr14:63249200-63253000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr14:63249200-63253200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr14:63250200-63253200	Weak transcription	HUES48 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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