Variant report

Variant	rs4580527
Chromosome Location	chr3:101258778-101258779
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1019677	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13322987	0.86[AMR][1000 genomes]
rs16843927	0.86[AMR][1000 genomes]
rs1918405	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4287896	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6772703	0.86[AMR][1000 genomes]
rs7628681	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7631506	0.86[AMR][1000 genomes]
rs9814991	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4580527	SENP7	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101251800-101260800	Weak transcription	Primary T cells from cord blood	blood
2	chr3:101258200-101259200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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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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