Variant report

Variant	rs8127954
Chromosome Location	chr21:16491718-16491719
allele	A/G
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]
rs2002625	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2011751	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2011752	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61121249	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62218213	0.84[EUR][1000 genomes]
rs62218214	0.86[EUR][1000 genomes]
rs62218216	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8134766	0.84[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16491000-16491800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr21:16491400-16491800	Enhancers	Primary hematopoietic stem cells	blood
3	chr21:16491400-16491800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr21:16491400-16492200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr21:16491400-16492400	Enhancers	Fetal Brain Female	brain
6	chr21:16491600-16491800	Enhancers	Duodenum Mucosa	Duodenum
7	chr21:16491600-16492200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr21:16491600-16492200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr21:16491600-16493200	Weak transcription	Fetal Brain Male	brain

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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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