Variant report

Variant	rs6482443
Chromosome Location	chr10:25060887-25060888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs2152432	0.83[EUR][1000 genomes]
rs4350272	0.80[EUR][1000 genomes]
rs4570483	0.83[EUR][1000 genomes]
rs4747498	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4747499	0.88[EUR][1000 genomes]
rs4747500	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4748977	0.84[EUR][1000 genomes]
rs4748978	0.84[EUR][1000 genomes]
rs4748981	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6482440	0.83[EUR][1000 genomes]
rs7911992	0.90[EUR][1000 genomes]
rs951857	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs951859	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs952917	0.98[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25060200-25063000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:25060600-25061600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr10:25060800-25062000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	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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