Variant report

Variant	rs78846115
Chromosome Location	chr15:74164680-74164681
allele	C/T
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	nsv1043335	chr15:74078689-74241186	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	esv3496464	chr15:74163499-74165397	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74154800-74167000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:74162600-74164800	Enhancers	Fetal Intestine Small	intestine
3	chr15:74163200-74164800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr15:74163600-74164800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr15:74163600-74165200	Enhancers	Osteobl	bone
6	chr15:74163600-74165600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr15:74163800-74164800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:74164400-74165200	Enhancers	NHDF-Ad	bronchial
9	chr15:74164600-74164800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
10	chr15:74164600-74164800	Enhancers	Left Ventricle	heart
11	chr15:74164600-74164800	Enhancers	Pancreas	Pancrea
12	chr15:74164600-74164800	Bivalent Enhancer	Stomach Mucosa	stomach
13	chr15:74164600-74165200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:74164600-74165200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr15:74164600-74167800	Weak transcription	Fetal Intestine Large	intestine

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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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