Variant report

Variant	rs2084130
Chromosome Location	chr5:60850467-60850468
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10035484	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10447098	1.00[CHD][hapmap]
rs153379	1.00[ASN][1000 genomes]
rs153380	1.00[ASN][1000 genomes]
rs153429	1.00[ASN][1000 genomes]
rs16892457	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17339983	1.00[CEU][hapmap]
rs251895	1.00[ASN][1000 genomes]
rs253531	1.00[ASN][1000 genomes]
rs253533	1.00[ASN][1000 genomes]
rs34404532	1.00[ASN][1000 genomes]
rs391101	1.00[ASN][1000 genomes]
rs436696	1.00[ASN][1000 genomes]
rs4416552	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4627943	0.87[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55816286	1.00[ASN][1000 genomes]
rs62366280	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62366281	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs860648	1.00[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60840200-60852200	Weak transcription	Left Ventricle	heart
2	chr5:60844000-60850800	Weak transcription	NHLF	lung

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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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