Variant report

Variant	rs570122151
Chromosome Location	chr15:49761032-49761033
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:49759384..49762245-chr15:49912531..49914153,2	MCF-7	breast:
2	chr15:49760434..49762831-chr15:49768683..49770217,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166262	Chromatin interaction
ENSG00000104047	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039368	chr15:49566094-49764066	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv833002	chr15:49621400-49781799	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv9263	chr15:49734435-49809465	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv974574	chr15:49752716-49764974	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1043119	chr15:49760222-49844366	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49752400-49764000	Weak transcription	HSMM	muscle
2	chr15:49755000-49764000	Weak transcription	Fetal Lung	lung
3	chr15:49755400-49764200	Weak transcription	Fetal Heart	heart
4	chr15:49758200-49761200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:49758200-49761200	Enhancers	Colon Smooth Muscle	Colon
6	chr15:49758200-49761600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr15:49758400-49761200	Enhancers	Hela-S3	cervix
8	chr15:49759400-49761200	Enhancers	NHLF	lung
9	chr15:49759600-49761200	Enhancers	Liver	Liver
10	chr15:49759600-49762800	Weak transcription	GM12878-XiMat	blood
11	chr15:49759600-49763800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr15:49759800-49761200	Enhancers	Rectal Smooth Muscle	rectum
13	chr15:49760400-49761200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr15:49760800-49761200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:49760800-49761200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr15:49761000-49761200	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr15:49761000-49761200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:49761000-49761200	Flanking Active TSS	NHDF-Ad	bronchial
19	chr15:49761000-49761200	Enhancers	Osteobl	bone
20	chr15:49761000-49764200	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr15:49761000-49766000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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