Variant report

Variant	rs35273195
Chromosome Location	chr9:108436091-108436092
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs13290324	0.82[EUR][1000 genomes]
rs13299856	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16924823	0.99[EUR][1000 genomes]
rs35073359	1.00[EUR][1000 genomes]
rs35171718	0.86[EUR][1000 genomes]
rs36016420	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9696805	0.85[AMR][1000 genomes];0.99[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	nsv519023	chr9:108371549-108454745	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	n/a
2	nsv893693	chr9:108427062-108683134	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108423600-108451600	Weak transcription	Psoas Muscle	Psoas
2	chr9:108433400-108436400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:108434400-108436200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr9:108434800-108436200	Enhancers	HepG2	liver
5	chr9:108434800-108436600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:108434800-108436600	Enhancers	K562	blood
7	chr9:108434800-108436800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr9:108434800-108437200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr9:108435000-108436800	Enhancers	Primary B cells from peripheral blood	blood
10	chr9:108435400-108436200	Enhancers	Liver	Liver
11	chr9:108435400-108436400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr9:108435800-108436400	Enhancers	Primary hematopoietic stem cells	blood
13	chr9:108435800-108436400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr9:108436000-108436600	Enhancers	GM12878-XiMat	blood

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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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