Variant report

Variant	rs73280851
Chromosome Location	chr14:69654281-69654282
allele	G/T
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]
rs1710993	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4902697	1.00[ASN][1000 genomes]
rs59946997	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6573870	0.86[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs66870630	1.00[ASN][1000 genomes]
rs8004546	0.89[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69650800-69657600	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr14:69651200-69657200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr14:69651200-69657400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:69651200-69657800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr14:69651400-69656800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr14:69651600-69657000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr14:69651600-69657400	Weak transcription	ES-I3 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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