Variant report

Variant	nsv71793
Chromosome Location	chr14:105338834-105338837
allele	n/a
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:1)
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	chr14:105282326..105284059-chr14:105337774..105340057,2	MCF-7	breast:
2	chr14:105264148..105266055-chr14:105338238..105340290,2	K562	blood:
3	chr14:105251130..105253358-chr14:105336625..105339105,2	MCF-7	breast:
4	chr14:105261883..105264033-chr14:105337531..105339628,2	MCF-7	breast:
5	chr14:105336666..105339518-chr14:105438239..105440025,2	MCF-7	breast:
6	chr14:105337863..105340802-chr14:105451441..105454537,3	MCF-7	breast:
7	chr14:105336757..105339297-chr14:105435240..105438194,2	MCF-7	breast:
8	chr14:105336440..105340478-chr14:105340944..105342699,3	MCF-7	breast:
9	chr14:105337782..105339687-chr14:105357084..105359181,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHNAK2-6	chr14:105338787-105339212	NONHSAT040303

No data

Variant related genes	Relation type
ENSG00000142208	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000140104	chromatin interactions

Extended variants
information (count: 2 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs398057473	chr14:105338834-105338835	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs375025948	chr14:105338835-105338836	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105333200-105342400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:105333200-105344200	Weak transcription	Aorta	Aorta
3	chr14:105333200-105346600	Weak transcription	Brain Angular Gyrus	brain
4	chr14:105333200-105346800	Weak transcription	Brain Substantia Nigra	brain
5	chr14:105333200-105346800	Weak transcription	A549	lung
6	chr14:105333200-105347200	Weak transcription	Left Ventricle	heart
7	chr14:105333400-105339200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr14:105333400-105344400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr14:105333400-105344400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr14:105333400-105344600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:105333400-105344800	Weak transcription	Brain Hippocampus Middle	brain
12	chr14:105333400-105349200	Weak transcription	Small Intestine	intestine
13	chr14:105333600-105346600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:105333600-105346600	Weak transcription	Colon Smooth Muscle	Colon
15	chr14:105333800-105343400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr14:105333800-105344400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr14:105334000-105346800	Weak transcription	Brain Anterior Caudate	brain
18	chr14:105334200-105351600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr14:105334400-105342400	Weak transcription	Hela-S3	cervix
20	chr14:105334400-105342400	Weak transcription	HepG2	liver
21	chr14:105334400-105348600	Weak transcription	Fetal Brain Male	brain
22	chr14:105334800-105339000	Strong transcription	Fetal Intestine Small	intestine
23	chr14:105336000-105342400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr14:105336200-105343600	Weak transcription	Brain Germinal Matrix	brain
25	chr14:105336200-105346600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr14:105336600-105339000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr14:105336600-105344200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr14:105336800-105339200	Genic enhancers	Pancreas	Pancrea
29	chr14:105336800-105340400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:105337000-105342400	Enhancers	Liver	Liver
31	chr14:105337200-105339000	Weak transcription	Fetal Intestine Large	intestine
32	chr14:105337600-105339000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:105337800-105339000	Enhancers	Right Ventricle	heart
34	chr14:105337800-105341600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr14:105338000-105339200	Enhancers	Stomach Smooth Muscle	stomach
36	chr14:105338000-105339600	Enhancers	Spleen	Spleen
37	chr14:105338000-105340600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr14:105338000-105342400	Enhancers	HMEC	breast
39	chr14:105338200-105339000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr14:105338200-105339200	Genic enhancers	Gastric	stomach
41	chr14:105338200-105341400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr14:105338200-105342600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr14:105338400-105339000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr14:105338400-105339000	Genic enhancers	Colonic Mucosa	Colon
45	chr14:105338400-105339200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr14:105338400-105339200	Enhancers	Duodenum Mucosa	Duodenum
47	chr14:105338400-105339400	Enhancers	Lung	lung
48	chr14:105338400-105339400	Flanking Active TSS	HSMM	muscle
49	chr14:105338400-105339600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:105338400-105339600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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