Variant report

Variant	rs553768158
Chromosome Location	chr9:16107174-16107175
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv429999	chr9:16102066-16389100	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv892638	chr9:16106659-16172580	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16099200-16107400	Enhancers	Fetal Muscle Leg	muscle
2	chr9:16099800-16107400	Enhancers	Fetal Stomach	stomach
3	chr9:16100400-16107200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:16102000-16108600	Enhancers	Fetal Lung	lung
5	chr9:16105000-16107400	Enhancers	Fetal Muscle Trunk	muscle
6	chr9:16106000-16107200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr9:16106200-16107200	Enhancers	Adipose Nuclei	Adipose
8	chr9:16106800-16107400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:16106800-16109200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:16107000-16108200	Weak transcription	Brain Substantia Nigra	brain

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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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