Variant report

Variant	rs11032417
Chromosome Location	chr11:33856402-33856403
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11032413	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12420267	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12797549	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12805407	0.82[EUR][1000 genomes]
rs4755340	0.83[EUR][1000 genomes]
rs4756025	0.83[EUR][1000 genomes]
rs4756052	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6416077	0.83[EUR][1000 genomes]
rs6484676	0.83[EUR][1000 genomes]
rs6484677	0.83[EUR][1000 genomes]
rs6484678	0.83[EUR][1000 genomes]
rs66951942	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7131427	0.83[EUR][1000 genomes]
rs7928022	0.83[EUR][1000 genomes]

No data

Chromatin state (count:9 , 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	chr11:33856200-33857000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:33856200-33857600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr11:33856200-33857600	Enhancers	NHDF-Ad	bronchial
8	chr11:33856400-33856600	Bivalent Enhancer	Hela-S3	cervix
9	chr11:33856400-33857600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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