Variant report

Variant	rs12435771
Chromosome Location	chr14:84565684-84565685
allele	C/G/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]
rs1381614	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1462348	0.84[ASN][1000 genomes]
rs1676052	0.81[ASN][1000 genomes]
rs1766151	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1766155	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1766157	0.83[ASN][1000 genomes]
rs1779556	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1779559	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1779561	0.83[ASN][1000 genomes]
rs1779562	0.83[ASN][1000 genomes]
rs1779567	0.84[ASN][1000 genomes]
rs1779568	0.83[ASN][1000 genomes]
rs2787459	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7146928	0.84[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84558600-84566400	Weak transcription	Fetal Stomach	stomach
2	chr14:84565200-84566200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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