Variant report

Variant	rs73133918
Chromosome Location	chr5:94099954-94099955
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs13359541	0.90[EUR][1000 genomes]
rs17084095	0.90[EUR][1000 genomes]
rs57297740	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57663699	0.89[ASN][1000 genomes]
rs58209835	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs59357233	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61327121	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6867377	0.90[EUR][1000 genomes]
rs6888297	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73133942	0.89[ASN][1000 genomes]
rs73133946	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73133954	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7712065	0.89[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94074200-94127600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:94083000-94108000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr5:94083000-94125800	Weak transcription	HUVEC	blood vessel
4	chr5:94085200-94105800	Weak transcription	Fetal Thymus	thymus
5	chr5:94086200-94101800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr5:94087400-94100400	Weak transcription	Spleen	Spleen
7	chr5:94089600-94107800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr5:94097800-94128400	Weak transcription	Primary T cells from cord blood	blood

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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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