Variant report

Variant	rs57338369
Chromosome Location	chr13:51206289-51206290
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs55670628	0.87[AMR][1000 genomes]
rs56261461	0.87[AMR][1000 genomes]
rs74077828	0.87[AMR][1000 genomes]
rs74077860	0.87[AMR][1000 genomes]
rs74078107	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078113	1.00[AMR][1000 genomes]
rs74078122	0.87[AMR][1000 genomes]
rs74078125	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078127	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078633	0.87[AMR][1000 genomes]
rs7998341	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
2	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753864	chr13:51136699-51375199	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1045733	chr13:51187575-51217464	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51191600-51210800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:51201400-51209400	Weak transcription	Adipose Nuclei	Adipose
3	chr13:51204800-51206800	Weak transcription	Aorta	Aorta
4	chr13:51204800-51207600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr13:51204800-51208800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr13:51204800-51209800	Weak transcription	Fetal Lung	lung
7	chr13:51205600-51206600	Weak transcription	HUVEC	blood vessel
8	chr13:51205600-51209600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:51205600-51209800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:51205800-51209200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr13:51206200-51211200	Enhancers	Primary monocytes fromperipheralblood	blood

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

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