Variant report

Variant	rs4902821
Chromosome Location	chr14:70920997-70920998
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11846259	0.95[ASN][1000 genomes]
rs1892282	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2050720	0.95[ASN][1000 genomes]
rs2877662	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2877663	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4641669	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4899352	0.97[ASN][1000 genomes]
rs61979082	0.80[AFR][1000 genomes]
rs7160442	0.86[EUR][1000 genomes]
rs74062713	0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70908800-70921600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr14:70910600-70955600	Weak transcription	Left Ventricle	heart
3	chr14:70913200-70921600	Weak transcription	Adipose Nuclei	Adipose
4	chr14:70913800-70921400	Weak transcription	Ovary	ovary
5	chr14:70916600-70921600	Weak transcription	Psoas Muscle	Psoas
6	chr14:70917000-70921000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr14:70917000-70940200	Weak transcription	Aorta	Aorta
8	chr14:70919800-70922000	Enhancers	Fetal Heart	heart
9	chr14:70920600-70922200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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