Variant report

Variant	rs11082530
Chromosome Location	chr18:44088840-44088841
allele	G/T
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]
rs1020568	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11082531	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1450428	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1450429	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1450430	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2282552	0.91[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs2282553	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28584347	0.89[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4890665	0.99[ASN][1000 genomes]
rs56210200	0.89[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs61257029	0.87[AFR][1000 genomes];0.84[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44086000-44114400	Weak transcription	Spleen	Spleen
2	chr18:44086800-44090800	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr18:44086800-44099200	Weak transcription	Right Ventricle	heart
4	chr18:44088000-44096400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr18:44088400-44090400	Strong 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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