Variant report

Variant	rs35229401
Chromosome Location	chr1:179662877-179662878
allele	C/T
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]
rs10157699	0.91[EUR][1000 genomes]
rs10798711	0.84[EUR][1000 genomes]
rs12747675	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17369945	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35448215	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4628468	0.91[EUR][1000 genomes]
rs4652418	0.80[EUR][1000 genomes]
rs4652426	0.83[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs61826402	0.83[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs61826427	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179661800-179663600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr1:179662600-179669600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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