Variant report

Variant	rs1432843
Chromosome Location	chr5:146895028-146895029
allele	A/C
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]
rs1368366	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs1368367	0.96[CEU][hapmap];0.98[EUR][1000 genomes]
rs1432844	0.99[EUR][1000 genomes]
rs2032857	0.99[EUR][1000 genomes]
rs60291144	0.90[EUR][1000 genomes]
rs62379598	0.95[EUR][1000 genomes]
rs6580464	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs6580466	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6580468	0.99[EUR][1000 genomes]
rs6880491	0.98[EUR][1000 genomes]
rs7706630	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146890200-146895200	Weak transcription	HUVEC	blood vessel
2	chr5:146890200-146901200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr5:146890200-146901200	Weak transcription	NHLF	lung
4	chr5:146890200-146901600	Weak transcription	NHDF-Ad	bronchial
5	chr5:146892200-146898800	Weak transcription	Brain Germinal Matrix	brain

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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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