Variant report

Variant	rs74047153
Chromosome Location	chr13:38327146-38327147
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1155260	1.00[EUR][1000 genomes]
rs1413001	1.00[EUR][1000 genomes]
rs7321803	1.00[EUR][1000 genomes]
rs74047130	1.00[EUR][1000 genomes]
rs74047131	1.00[EUR][1000 genomes]
rs74047132	0.83[AFR][1000 genomes]
rs74047135	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047138	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047139	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047141	1.00[EUR][1000 genomes]
rs74047142	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047144	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047148	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047152	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74047157	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74047159	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74049742	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs963953	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045716	chr13:37952062-38394595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr13:38307600-38330800	Weak transcription	Ovary	ovary
2	chr13:38308200-38328200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr13:38316000-38328200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:38320400-38330800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:38322400-38327800	Weak transcription	Osteobl	bone
6	chr13:38326400-38327200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:38326600-38327200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr13:38326800-38327400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:38326800-38328600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr13:38327000-38327400	Weak transcription	Brain Anterior Caudate	brain
11	chr13:38327000-38328200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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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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