Variant report

Variant	rs11053569
Chromosome Location	chr12:10202639-10202640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10505751	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12582351	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17205644	0.93[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4764227	0.90[ASN][1000 genomes]
rs61918591	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61918592	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61918593	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61918595	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7136826	0.90[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs874463	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10195400-10203800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:10201800-10204200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr12:10201800-10204200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:10202000-10203800	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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