Variant report

Variant	rs548611702
Chromosome Location	chr3:70093364-70093365
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv533396	chr3:69964029-70538306	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	esv3375671	chr3:70093362-70095360	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70063800-70098000	Weak transcription	Aorta	Aorta
2	chr3:70090000-70093600	Weak transcription	Brain Anterior Caudate	brain
3	chr3:70091000-70093800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr3:70091200-70093400	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr3:70091600-70093400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:70092000-70105000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:70092400-70093800	Enhancers	Brain Germinal Matrix	brain
8	chr3:70092800-70093600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:70092800-70093800	Enhancers	Brain Hippocampus Middle	brain
10	chr3:70093200-70093800	Enhancers	Brain Angular Gyrus	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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