Variant report

Variant	rs34244999
Chromosome Location	chr1:223724740-223724741
allele	A/G
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:10)

rs_ID	r²[population]
rs34157106	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34158997	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34267716	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34897445	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35808016	0.81[EUR][1000 genomes]
rs35916490	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4072246	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61823525	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61823552	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61825160	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][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	nsv832681	chr1:223698048-224002691	Strong transcription Active TSS Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv873209	chr1:223707647-223846564	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv873210	chr1:223707647-223856414	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv873211	chr1:223707647-223867631	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr1:223714400-223728200	Weak transcription	Fetal Stomach	stomach
2	chr1:223718600-223727000	Weak transcription	Gastric	stomach
3	chr1:223723400-223725000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:223723400-223725600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr1:223723400-223725600	Enhancers	Stomach Mucosa	stomach
6	chr1:223723400-223725600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr1:223724000-223724800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:223724000-223725000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr1:223724000-223725400	Enhancers	Primary B cells from peripheral blood	blood
10	chr1:223724000-223725400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr1:223724600-223724800	Enhancers	GM12878-XiMat	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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