Variant report

Variant	rs73656706
Chromosome Location	chr9:117713417-117713418
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs73656707	1.00[AFR][1000 genomes]
rs73656708	0.94[AFR][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	nsv831695	chr9:117567626-117726247	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv831696	chr9:117701582-117874150	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117708600-117714000	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr9:117709800-117714000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr9:117710600-117715400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:117710800-117715600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr9:117711800-117715400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr9:117713000-117713800	Enhancers	Fetal Lung	lung
7	chr9:117713000-117714000	Enhancers	Liver	Liver
8	chr9:117713200-117713600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:117713200-117713600	Enhancers	Primary hematopoietic stem cells short term culture	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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