Variant report

Variant	rs74133311
Chromosome Location	chr10:54091725-54091726
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs55911116	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56342850	0.94[AFR][1000 genomes]
rs59411921	1.00[AMR][1000 genomes]
rs59563498	1.00[AMR][1000 genomes]
rs61160703	1.00[AMR][1000 genomes]
rs61276082	1.00[AMR][1000 genomes]
rs7072159	1.00[AMR][1000 genomes]
rs73331289	1.00[AMR][1000 genomes]
rs73333105	1.00[AMR][1000 genomes]
rs73339097	1.00[AMR][1000 genomes]
rs73341105	1.00[AMR][1000 genomes]
rs74133309	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133310	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74133313	1.00[AMR][1000 genomes]
rs74133314	1.00[AMR][1000 genomes]
rs74133315	1.00[AMR][1000 genomes]
rs74133318	1.00[AMR][1000 genomes]
rs74135373	1.00[AMR][1000 genomes]
rs74135375	1.00[AMR][1000 genomes]
rs74135378	1.00[AMR][1000 genomes]
rs74135379	1.00[AMR][1000 genomes]
rs74135381	1.00[AMR][1000 genomes]
rs74135382	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv895399	chr10:53900872-54219820	Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv895400	chr10:54073294-54094359	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54078400-54094800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr10:54078600-54093200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:54083200-54094400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr10:54084000-54094000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr10:54086000-54093200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr10:54086400-54093200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr10:54086400-54097400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr10:54090600-54092600	Enhancers	A549	lung
9	chr10:54090600-54094000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr10:54091200-54091800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr10:54091200-54092000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr10:54091400-54092000	Enhancers	Duodenum Mucosa	Duodenum
13	chr10:54091400-54092200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:54091400-54092200	Enhancers	Fetal Intestine Large	intestine
15	chr10:54091400-54092600	Enhancers	Fetal Intestine Small	intestine
16	chr10:54091400-54095200	Enhancers	HepG2	liver
17	chr10:54091600-54094000	Enhancers	HUVEC	blood vessel

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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