Variant report

Variant	rs114078380
Chromosome Location	chr5:68812965-68812966
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:68664276..68666679-chr5:68812958..68815555,2	MCF-7	breast:
2	chr5:68811437..68815245-chr5:68822688..68826346,4	MCF-7	breast:
3	chr5:68808067..68811530-chr5:68811540..68813490,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000085231	Chromatin interaction
ENSG00000152942	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018410	chr5:68692244-68822384	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1023116	chr5:68744307-68867282	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1034024	chr5:68760271-69118123	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv1804444	chr5:68812530-68838432	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	esv1818827	chr5:68812530-68849594	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv1832055	chr5:68812530-68849594	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68790200-68824600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:68793200-68813600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr5:68799000-68823200	Weak transcription	Placenta	Placenta
4	chr5:68799400-68814200	Weak transcription	Colonic Mucosa	Colon
5	chr5:68799400-68821800	Weak transcription	Fetal Stomach	stomach
6	chr5:68805400-68813000	Weak transcription	Esophagus	oesophagus
7	chr5:68805600-68816400	Weak transcription	GM12878-XiMat	blood
8	chr5:68805600-68821600	Weak transcription	Lung	lung
9	chr5:68805600-68823400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:68805600-68826200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:68805600-68826600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr5:68806000-68824200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr5:68806400-68826400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:68806800-68816800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:68806800-68821400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr5:68807000-68821400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:68807000-68821600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr5:68809000-68814200	Weak transcription	Small Intestine	intestine
19	chr5:68809200-68816400	Weak transcription	NHEK	skin
20	chr5:68809200-68817000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr5:68809600-68813400	Weak transcription	NH-A	brain
22	chr5:68809600-68813600	Weak transcription	NHDF-Ad	bronchial
23	chr5:68809600-68814200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr5:68809600-68814600	Weak transcription	Pancreas	Pancrea
25	chr5:68809600-68817200	Weak transcription	NHLF	lung
26	chr5:68809800-68816600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:68810000-68813400	Weak transcription	Duodenum Mucosa	Duodenum
28	chr5:68810400-68815200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr5:68810400-68815600	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr5:68810400-68815600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:68810400-68821600	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr5:68810400-68821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr5:68810400-68823600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:68812000-68813000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:68812000-68813400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr5:68812200-68815200	Enhancers	Hela-S3	cervix
37	chr5:68812200-68818000	Enhancers	Stomach Mucosa	stomach
38	chr5:68812400-68813000	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr5:68812400-68813400	Enhancers	A549	lung
40	chr5:68812400-68813800	Enhancers	HMEC	breast
41	chr5:68812400-68814400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:68812400-68814400	Enhancers	HUVEC	blood vessel
43	chr5:68812400-68814600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:68812400-68814600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr5:68812400-68814600	Enhancers	Osteobl	bone
46	chr5:68812400-68814800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:68812400-68815600	Enhancers	Fetal Intestine Large	intestine
48	chr5:68812400-68816000	Enhancers	Liver	Liver
49	chr5:68812600-68813000	Genic enhancers	Fetal Intestine Small	intestine
50	chr5:68812600-68814200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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