Variant report

Variant	rs11032416
Chromosome Location	chr11:33856178-33856179
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10836110	0.85[CEU][hapmap]
rs10836119	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11032397	0.95[CEU][hapmap];0.86[EUR][1000 genomes]
rs11032408	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1522084	0.84[CEU][hapmap]
rs4756002	0.84[CEU][hapmap]
rs66535760	0.82[EUR][1000 genomes]
rs7109097	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7115489	0.95[CEU][hapmap]
rs884710	0.84[CEU][hapmap]
rs953142	0.84[CEU][hapmap]
rs999479	0.94[CEU][hapmap];0.84[EUR][1000 genomes]

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11032416	CD59	Cis_1M	lymphoblastoid	RTeQTL
rs11032416	CD59	cis	Artery Tibial	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33853200-33856600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:33853200-33857000	Weak transcription	NHEK	skin
3	chr11:33853400-33856600	Weak transcription	HMEC	breast
4	chr11:33853400-33857000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:33856000-33856400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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