Variant report

Variant	rs1603983
Chromosome Location	chr3:25149547-25149548
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1587426	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1603984	1.00[ASN][1000 genomes]
rs1603985	1.00[ASN][1000 genomes]
rs1603986	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34850898	0.85[AFR][1000 genomes]
rs6550949	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66831722	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9826164	0.86[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25147600-25152200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:25147800-25157600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:25148600-25149600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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