Variant report

Variant	rs567299816
Chromosome Location	chr3:78745169-78745170
allele	C/T
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	nsv1008156	chr3:78444137-78765884	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv1010804	chr3:78739648-79087470	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv1842222	chr3:78744206-78778901	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr3:78654200-78746600	Weak transcription	NHDF-Ad	bronchial
2	chr3:78667200-78751200	Weak transcription	Esophagus	oesophagus
3	chr3:78717800-78745200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:78717800-78748400	Weak transcription	Ovary	ovary
5	chr3:78719600-78753000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:78720000-78753200	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:78730400-78752600	Weak transcription	Fetal Stomach	stomach
8	chr3:78733800-78746600	Weak transcription	Fetal Lung	lung
9	chr3:78733800-78752400	Weak transcription	Fetal Kidney	kidney
10	chr3:78733800-78778000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr3:78735200-78765600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr3:78740400-78773800	Weak transcription	Brain Germinal Matrix	brain
13	chr3:78740600-78756200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr3:78742600-78756400	Weak transcription	HepG2	liver

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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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