Variant report

Variant	rs4725401
Chromosome Location	chr7:151013043-151013044
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1012007	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1012008	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12535753	0.86[ASN][1000 genomes]
rs12539643	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2792440	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs401168	0.80[ASN][1000 genomes]
rs438906	0.80[ASN][1000 genomes]
rs73171826	0.88[ASN][1000 genomes]
rs760234	1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs887018	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs909210	1.00[YRI][hapmap];0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:151010800-151015800	Weak transcription	Right Atrium	heart
2	chr7:151012200-151014400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr7:151012200-151014400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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