Variant report

Variant	rs35715037
Chromosome Location	chr11:121226532-121226533
allele	C/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]
rs12275074	0.85[ASN][1000 genomes]
rs1529578	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs297528	0.93[ASN][1000 genomes]
rs4936618	1.00[ASN][1000 genomes]
rs4936621	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6589878	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7111793	0.90[ASN][1000 genomes]
rs7114702	0.87[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121221600-121228200	Weak transcription	Pancreas	Pancrea
2	chr11:121224000-121228200	Weak transcription	Left Ventricle	heart
3	chr11:121224000-121230800	Weak transcription	Right Atrium	heart
4	chr11:121224200-121236000	Weak transcription	Fetal Brain Female	brain
5	chr11:121224600-121229600	Weak transcription	Fetal Brain Male	brain
6	chr11:121225000-121228400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr11:121225200-121227600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr11:121225400-121226800	Enhancers	Stomach Mucosa	stomach
9	chr11:121225600-121227200	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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