Variant report

Variant	rs55957667
Chromosome Location	chr14:69407295-69407296
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69402982..69422523-chr14:69436263..69448017,46	MCF-7	breast:
2	chr14:69256868..69259474-chr14:69407183..69409516,2	MCF-7	breast:
3	chr14:69391196..69393563-chr14:69405048..69407847,2	MCF-7	breast:
4	chr14:69403117..69416483-chr14:69441657..69449888,50	MCF-7	breast:
5	chr14:69398641..69402402-chr14:69406063..69410861,5	MCF-7	breast:
6	chr14:69404468..69406535-chr14:69406823..69410783,6	MCF-7	breast:
7	chr14:69404437..69408069-chr14:69415844..69420142,4	MCF-7	breast:
8	chr14:69402918..69410408-chr14:69410942..69415819,17	MCF-7	breast:
9	chr14:69388864..69393027-chr14:69403394..69408215,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259062	Chromatin interaction
ENSG00000185650	Chromatin interaction
ENSG00000072110	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs56038222	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7148988	1.00[ASN][1000 genomes]
rs7152850	1.00[ASN][1000 genomes]
rs72733540	1.00[ASN][1000 genomes]
rs8003964	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832823	chr14:69388853-69567638	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv564964	chr14:69392264-69423164	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv456333	chr14:69392445-69415962	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv564965	chr14:69392445-69415962	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69387400-69420400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr14:69394200-69422200	Weak transcription	Dnd41	blood
3	chr14:69396200-69408800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr14:69396400-69409000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:69397800-69415200	Enhancers	Esophagus	oesophagus
6	chr14:69399000-69423200	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr14:69399400-69407600	Genic enhancers	NHEK	skin
8	chr14:69400000-69408400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:69400200-69416400	Enhancers	Pancreas	Pancrea
10	chr14:69400400-69417000	Enhancers	Fetal Muscle Leg	muscle
11	chr14:69400800-69420400	Enhancers	Fetal Lung	lung
12	chr14:69401200-69408400	Enhancers	Muscle Satellite Cultured Cells	--
13	chr14:69401800-69412400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr14:69402000-69426200	Enhancers	Primary T cells fromperipheralblood	blood
15	chr14:69402200-69425200	Enhancers	Right Atrium	heart
16	chr14:69402400-69407400	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr14:69402400-69407400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr14:69402400-69407600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr14:69402400-69407800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr14:69402400-69409000	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr14:69402400-69409800	Enhancers	Lung	lung
22	chr14:69402400-69414400	Enhancers	Adipose Nuclei	Adipose
23	chr14:69402400-69416400	Enhancers	Left Ventricle	heart
24	chr14:69402400-69423600	Enhancers	Fetal Heart	heart
25	chr14:69402400-69427000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr14:69402600-69410800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr14:69402600-69416600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr14:69403400-69407800	Enhancers	Colonic Mucosa	Colon
29	chr14:69403600-69409400	Enhancers	Brain Hippocampus Middle	brain
30	chr14:69403600-69409600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr14:69403600-69420400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:69403800-69407400	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr14:69403800-69408400	Enhancers	Fetal Intestine Large	intestine
34	chr14:69403800-69411400	Enhancers	Placenta Amnion	Placenta Amnion
35	chr14:69404200-69407600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr14:69404200-69408200	Enhancers	NHDF-Ad	bronchial
37	chr14:69404200-69409800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:69404200-69410400	Flanking Active TSS	A549	lung
39	chr14:69404200-69412600	Enhancers	Fetal Muscle Trunk	muscle
40	chr14:69404200-69417000	Enhancers	Right Ventricle	heart
41	chr14:69404400-69411000	Enhancers	Placenta	Placenta
42	chr14:69404400-69411800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr14:69404600-69410800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:69404600-69412200	Weak transcription	K562	blood
45	chr14:69404800-69409000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr14:69404800-69409400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr14:69404800-69409600	Weak transcription	Thymus	Thymus
48	chr14:69405000-69415400	Weak transcription	Psoas Muscle	Psoas
49	chr14:69405200-69408000	Enhancers	HSMMtube	muscle
50	chr14:69405200-69408400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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