Variant report

Variant	rs34254603
Chromosome Location	chr3:133770802-133770803
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs13058950	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13062864	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13096547	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4274739	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7621667	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133770600-133771600	Enhancers	Lung	lung
2	chr3:133770800-133771200	Enhancers	Spleen	Spleen
3	chr3:133770800-133771400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:133770800-133771600	Enhancers	Adipose Nuclei	Adipose
5	chr3:133770800-133771600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
6	chr3:133770800-133771600	Enhancers	Right Atrium	heart

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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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