Variant report

Variant	rs1766151
Chromosome Location	chr14:84555125-84555126
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12435771	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12437025	0.83[ASN][1000 genomes]
rs1381614	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1462348	0.92[ASN][1000 genomes]
rs1564057	0.81[ASN][1000 genomes]
rs1676052	0.98[ASN][1000 genomes]
rs1766153	0.99[ASN][1000 genomes]
rs1766155	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1766157	0.95[ASN][1000 genomes]
rs1779555	0.99[ASN][1000 genomes]
rs1779556	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1779558	0.99[ASN][1000 genomes]
rs1779559	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1779561	0.95[ASN][1000 genomes]
rs1779562	0.95[ASN][1000 genomes]
rs1779567	0.92[ASN][1000 genomes]
rs1779568	0.91[ASN][1000 genomes]
rs2787459	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7146928	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84550600-84558400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:84550600-84563800	Weak transcription	Esophagus	oesophagus
3	chr14:84551600-84556800	Weak transcription	Adipose Nuclei	Adipose
4	chr14:84553600-84555400	Enhancers	Fetal Stomach	stomach
5	chr14:84554600-84557200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr14:84554800-84556800	Weak transcription	Ovary	ovary

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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