Variant report

Variant	rs16925213
Chromosome Location	chr10:25285517-25285518
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11014310	1.00[AMR][1000 genomes]
rs1158057	1.00[AMR][1000 genomes]
rs12098488	1.00[AMR][1000 genomes]
rs1352983	0.83[YRI][hapmap]
rs16925204	1.00[AMR][1000 genomes]
rs16925206	1.00[AMR][1000 genomes]
rs16925221	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16925231	0.83[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34736361	1.00[AMR][1000 genomes]
rs3920009	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7091416	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7901799	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25264600-25292200	Weak transcription	Ovary	ovary
2	chr10:25282200-25287800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr10:25283000-25286800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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