Variant report

Variant	rs535846210
Chromosome Location	chr5:14914604-14914605
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFYB	chr5:14914301-14914738	K562	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000212036	TF binding region

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018187	chr5:14385164-15127103	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv830212	chr5:14784197-14966683	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	esv2755538	chr5:14814900-14927500	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	nsv530221	chr5:14859687-15364470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv432717	chr5:14887400-15126500	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1017579	chr5:14888997-15194335	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv597261	chr5:14913369-14962587	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 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	chr5:14911000-14914800	Weak transcription	Fetal Heart	heart
2	chr5:14912000-14916400	Enhancers	Placenta Amnion	Placenta Amnion
3	chr5:14912000-14919200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr5:14912600-14915600	Enhancers	Osteobl	bone
5	chr5:14913000-14916200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:14913000-14916400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:14913800-14914800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:14913800-14914800	Weak transcription	HSMMtube	muscle
9	chr5:14914000-14915600	Weak transcription	Placenta	Placenta
10	chr5:14914400-14914800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr5:14914400-14916000	Enhancers	NHDF-Ad	bronchial
12	chr5:14914400-14916200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr5:14914400-14916200	Enhancers	Hela-S3	cervix
14	chr5:14914400-14916400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:14914400-14916800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:14914400-14919000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:14914400-14919000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr5:14914600-14914800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr5:14914600-14916400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:14914600-14916600	Enhancers	HepG2	liver
21	chr5:14914600-14916600	Enhancers	NH-A	brain

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