Variant report

Variant	rs4641669
Chromosome Location	chr14:70920380-70920381
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11846259	0.97[ASN][1000 genomes]
rs1892282	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2050720	0.97[ASN][1000 genomes]
rs2877662	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2877663	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4899352	1.00[ASN][1000 genomes]
rs4902821	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7160442	0.85[EUR][1000 genomes]
rs74062713	0.98[ASN][1000 genomes]

No data

Chromatin state (count:8 , 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

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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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