Variant report

Variant	rs11590937
Chromosome Location	chr1:211883505-211883506
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12729804	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12742934	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12747691	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35768943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6669055	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7513065	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7540628	0.84[EUR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211872800-211884000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:211879200-211884600	Weak transcription	Esophagus	oesophagus
3	chr1:211879200-211913600	Weak transcription	Right Atrium	heart
4	chr1:211879400-211884000	Weak transcription	Spleen	Spleen
5	chr1:211880000-211883600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr1:211880200-211884600	Weak transcription	NHEK	skin
7	chr1:211880400-211884600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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