Variant report

Variant	rs73133908
Chromosome Location	chr5:94085726-94085727
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs73133904	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73150143	1.00[ASN][1000 genomes]
rs73150166	1.00[ASN][1000 genomes]
rs73150174	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9791080	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94072600-94086200	Weak transcription	Spleen	Spleen
2	chr5:94074200-94127600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:94082400-94086200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:94082800-94086400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:94083000-94088000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr5:94083000-94108000	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr5:94083000-94125800	Weak transcription	HUVEC	blood vessel
8	chr5:94084800-94085800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr5:94084800-94088600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr5:94085000-94090400	Weak transcription	Hela-S3	cervix
11	chr5:94085200-94105800	Weak transcription	Fetal Thymus	thymus
12	chr5:94085400-94087600	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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