Variant report

Variant	rs13021288
Chromosome Location	chr2:37388656-37388657
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10181241	0.80[ASN][1000 genomes]
rs10204828	0.80[ASN][1000 genomes]
rs35349768	0.91[ASN][1000 genomes]
rs3891003	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6720068	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13021288	CEBPZ	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37385800-37389000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr2:37388600-37389400	Enhancers	HepG2	liver

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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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