Variant report

Variant	rs3891003
Chromosome Location	chr2:37398088-37398089
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10182759	0.80[JPT][hapmap]
rs10184179	0.93[JPT][hapmap]
rs11569755	0.80[CEU][hapmap];0.89[JPT][hapmap]
rs13018873	0.80[CEU][hapmap];0.82[JPT][hapmap]
rs13021288	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs13022271	0.87[JPT][hapmap]
rs35349768	0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3770749	0.88[YRI][hapmap]
rs3770752	0.86[JPT][hapmap]
rs4670667	0.87[JPT][hapmap]
rs6544062	0.80[JPT][hapmap]
rs6720068	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6724820	0.87[JPT][hapmap]
rs7565331	0.82[JPT][hapmap]
rs876462	1.00[JPT][hapmap]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3891003	CEBPZ	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37395600-37398400	Weak transcription	Stomach Mucosa	stomach
2	chr2:37395600-37398400	Weak transcription	HepG2	liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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