Variant report

Variant	rs579248
Chromosome Location	chr11:59634519-59634520
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1042613	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10896996	0.92[EUR][1000 genomes]
rs12274522	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs503644	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs515178	0.84[AMR][1000 genomes]
rs519221	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs537545	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs557564	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59633200-59634800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:59633800-59634600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr11:59634200-59636000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr11:59634400-59642600	Weak transcription	Hela-S3	cervix

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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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