Variant report

Variant	rs547758322
Chromosome Location	chr9:8555207-8555208
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv892228	chr9:8482778-8703733	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv831504	chr9:8496277-8665773	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1026208	chr9:8534915-8595338	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv973831	chr9:8554250-8557126	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8420600-8557600	Weak transcription	Aorta	Aorta
2	chr9:8534600-8564000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr9:8541600-8557600	Weak transcription	Fetal Stomach	stomach
4	chr9:8545600-8555800	Weak transcription	Fetal Lung	lung
5	chr9:8546000-8557000	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:8553000-8561400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:8553400-8555400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:8553600-8571000	Weak transcription	Brain Anterior Caudate	brain
9	chr9:8553800-8555800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr9:8553800-8555800	Weak transcription	Brain Substantia Nigra	brain
11	chr9:8553800-8559400	Weak transcription	Brain Angular Gyrus	brain
12	chr9:8554400-8555600	Weak transcription	Ovary	ovary
13	chr9:8554400-8557200	Enhancers	Liver	Liver
14	chr9:8555200-8555400	Enhancers	Fetal Muscle Trunk	muscle
15	chr9:8555200-8556200	Enhancers	Brain Hippocampus Middle	brain
16	chr9:8555200-8556400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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