Variant report

Variant	rs114238530
Chromosome Location	chr13:76301101-76301102
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv949152	chr13:76211453-76366622	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv900579	chr13:76244056-76307981	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1091	chr13:76282392-76327906	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv976261	chr13:76297598-76301199	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	n/a	n/a	inside rSNPs	diseases
5	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76279400-76308000	Weak transcription	Left Ventricle	heart
2	chr13:76283600-76308000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:76294800-76321800	Weak transcription	NH-A	brain
4	chr13:76297800-76301400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr13:76297800-76301400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr13:76298000-76301400	Enhancers	Stomach Mucosa	stomach
7	chr13:76298400-76301200	Enhancers	Fetal Lung	lung
8	chr13:76298600-76309200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr13:76298600-76313000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr13:76298600-76318800	Weak transcription	Gastric	stomach
11	chr13:76299200-76307800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr13:76299200-76308000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr13:76299400-76307800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr13:76299600-76310400	Weak transcription	NHLF	lung
15	chr13:76299800-76313000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr13:76300000-76301400	Weak transcription	Fetal Intestine Large	intestine
17	chr13:76300200-76301200	Enhancers	HSMMtube	muscle
18	chr13:76300200-76309200	Weak transcription	NHDF-Ad	bronchial
19	chr13:76300200-76313000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr13:76300400-76301400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:76300400-76301400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr13:76300600-76301400	Enhancers	Fetal Kidney	kidney
23	chr13:76300800-76301200	Enhancers	Fetal Intestine Small	intestine
24	chr13:76300800-76301200	Flanking Active TSS	Hela-S3	cervix
25	chr13:76300800-76301400	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr13:76300800-76301400	Strong transcription	Osteobl	bone
27	chr13:76301000-76301200	Enhancers	Placenta Amnion	Placenta Amnion
28	chr13:76301000-76301400	Genic enhancers	HSMM	muscle

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