Variant report

Variant	rs77636792
Chromosome Location	chr5:95964895-95964896
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	chr5:95962754..95968222-chr5:95995730..96000718,6	MCF-7	breast:
2	chr5:95962343..95964474-chr5:95964579..95968462,3	K562	blood:

Variant related genes	Relation type
ENSG00000153113	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	nsv1030444	chr5:95353620-95995619	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
2	nsv537810	chr5:95353620-95995619	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1024964	chr5:95742124-96065492	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv537811	chr5:95742124-96065492	Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
5	esv3470561	chr5:95964796-95969194	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95951400-95965000	Weak transcription	HUVEC	blood vessel
2	chr5:95954000-95965400	Weak transcription	Aorta	Aorta
3	chr5:95958400-95965400	Weak transcription	NHLF	lung
4	chr5:95961200-95966200	Enhancers	HSMM	muscle
5	chr5:95961200-95966200	Enhancers	NH-A	brain
6	chr5:95961200-95966400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:95961200-95966600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:95961200-95967200	Enhancers	HMEC	breast
9	chr5:95961400-95967000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:95962000-95966200	Enhancers	HSMMtube	muscle
11	chr5:95962000-95966400	Enhancers	Osteobl	bone
12	chr5:95962200-95967000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr5:95962400-95965600	Weak transcription	Right Atrium	heart
14	chr5:95962600-95965000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:95963400-95965000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:95963400-95966400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:95963400-95966800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:95963400-95967000	Enhancers	Hela-S3	cervix
19	chr5:95963800-95965000	Enhancers	NHEK	skin
20	chr5:95963800-95965200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:95964200-95965200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:95964200-95965400	Enhancers	Fetal Lung	lung
23	chr5:95964200-95966200	Enhancers	Stomach Mucosa	stomach
24	chr5:95964400-95965000	Enhancers	Fetal Heart	heart
25	chr5:95964400-95965400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:95964600-95965000	Enhancers	Esophagus	oesophagus
27	chr5:95964600-95965000	Weak transcription	HepG2	liver
28	chr5:95964600-95965000	Weak transcription	NHDF-Ad	bronchial
29	chr5:95964600-95965400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr5:95964800-95965600	Enhancers	A549	lung
31	chr5:95964800-95966400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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