Variant report

Variant	esv1821679
Chromosome Location	chr14:104991128-105037557
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:48)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105018505..105021042-chr14:105030444..105032502,2	MCF-7	breast:
2	chr14:105025262..105028783-chr14:105030319..105032347,4	MCF-7	breast:
3	chr14:105006694..105010475-chr14:105012280..105015827,3	MCF-7	breast:
4	chr14:104603560..104604807-chr14:105030044..105030981,6	MCF-7	breast:
5	chr14:104824690..104827500-chr14:105019187..105021176,2	MCF-7	breast:
6	chr14:104578163..104580512-chr14:105027254..105029393,2	MCF-7	breast:
7	chr14:104597425..104598274-chr14:105030009..105030913,3	MCF-7	breast:
8	chr14:105013872..105015383-chr14:105019169..105021029,2	K562	blood:
9	chr14:105034085..105038904-chr14:105041483..105045004,4	MCF-7	breast:
10	chr14:104694080..104694805-chr14:105030047..105031033,2	MCF-7	breast:
11	chr14:105016071..105018557-chr14:105018817..105021096,3	K562	blood:
12	chr14:104603333..104605492-chr14:105030428..105032769,2	MCF-7	breast:
13	chr14:104602285..104604606-chr14:105027289..105030127,2	MCF-7	breast:
14	chr14:105027918..105029787-chr14:105034276..105037133,2	MCF-7	breast:
15	chr14:104989297..104991322-chr14:104992411..104994539,2	MCF-7	breast:
16	chr14:105035401..105038783-chr14:105042040..105045385,3	MCF-7	breast:
17	chr14:105022528..105025531-chr14:105027060..105029977,3	K562	blood:
18	chr14:105027918..105029787-chr14:105034276..105037133,2	MCF-7	breast:
19	chr14:105013872..105015383-chr14:105019169..105021029,2	K562	blood:
20	chr14:104599830..104602632-chr14:105024556..105026842,2	MCF-7	breast:
21	chr14:105017921..105022172-chr14:105022189..105024897,5	MCF-7	breast:
22	chr14:104602607..104605303-chr14:105029346..105032032,3	MCF-7	breast:
23	chr14:105032385..105034173-chr14:105061495..105063938,2	K562	blood:
24	chr14:105022528..105025531-chr14:105027060..105029977,3	K562	blood:
25	chr14:104609989..104612052-chr14:105021237..105023581,2	MCF-7	breast:
26	chr14:104998567..105001306-chr14:105002948..105006156,3	MCF-7	breast:
27	chr14:105018505..105021042-chr14:105030444..105032502,2	MCF-7	breast:
28	chr14:105025262..105028783-chr14:105030319..105032347,4	MCF-7	breast:
29	chr14:104601077..104602107-chr14:105029674..105030837,6	MCF-7	breast:
30	chr14:104603534..104604192-chr14:105028243..105029014,2	MCF-7	breast:
31	chr14:104989297..104991322-chr14:104992411..104994539,2	MCF-7	breast:
32	chr14:105017921..105022172-chr14:105022189..105024897,5	MCF-7	breast:
33	chr14:105016071..105018557-chr14:105018817..105021096,3	K562	blood:
34	chr14:105017735..105019335-chr6:28831183..28833671,2	MCF-7	breast:
35	chr14:105017888..105020132-chr14:105106949..105108571,2	MCF-7	breast:
36	chr14:105030117..105031530-chr14:105105903..105107265,8	MCF-7	breast:
37	chr14:104597148..104597987-chr14:105029848..105030810,3	MCF-7	breast:
38	chr14:104544184..104544985-chr14:105029856..105031015,7	MCF-7	breast:
39	chr14:104998567..105001306-chr14:105002948..105006156,3	MCF-7	breast:
40	chr14:104603508..104604499-chr14:105029618..105031234,27	MCF-7	breast:
41	chr14:104808612..104811334-chr14:105028919..105032790,3	MCF-7	breast:
42	chr14:104603594..104604494-chr14:105016753..105017932,4	MCF-7	breast:
43	chr14:104544004..104544697-chr14:105030089..105031236,3	MCF-7	breast:
44	chr14:104544095..104545346-chr14:105030053..105031029,7	K562	blood:
45	chr14:105029275..105030973-chr14:105053381..105055372,2	MCF-7	breast:
46	chr14:104567251..104568942-chr14:105029276..105031338,2	MCF-7	breast:
47	chr14:105006694..105010475-chr14:105012280..105015827,3	MCF-7	breast:
48	chr14:105030217..105030977-chr14:105106374..105106938,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf180-3	chr14:104993418-104993777	expReg_chr14_7636_+

No data

Variant related genes	Relation type
ENSG00000258748	chromatin interactions
ENSG00000225595	chromatin interactions
ENSG00000066735	chromatin interactions

Extended variants
information (count: 2227 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2227 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375244921	chr14:104993009-104993010	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574893786	chr14:104993024-104993025	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115840343	chr14:104993053-104993054	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554101509	chr14:104993077-104993078	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71129237	chr14:104993091-104993092	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199877656	chr14:104993095-104993096	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546005257	chr14:104993102-104993103	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111888744	chr14:104993119-104993120	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111791685	chr14:104993120-104993121	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146019311	chr14:104993136-104993137	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376779059	chr14:104993141-104993142	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541571099	chr14:104993159-104993160	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4983584	chr14:104993161-104993162	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs370993482	chr14:104993178-104993179	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527288545	chr14:104993183-104993184	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372879175	chr14:104993197-104993198	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574509931	chr14:104993205-104993206	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs543129422	chr14:104993216-104993217	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs547030195	chr14:104993232-104993233	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566811340	chr14:104993235-104993236	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs532697890	chr14:104993238-104993239	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs553843093	chr14:104993246-104993247	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs552711917	chr14:104993251-104993252	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs569368498	chr14:104993254-104993255	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs71990589	chr14:104993269-104993270	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs56214026	chr14:104993270-104993271	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs398057467	chr14:104993274-104993275	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs538295050	chr14:104993282-104993283	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs554767414	chr14:104993289-104993290	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs568614268	chr14:104993292-104993293	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs534172287	chr14:104993299-104993300	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs545355265	chr14:104993302-104993303	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs367607969	chr14:104993305-104993306	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs371840463	chr14:104993307-104993308	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs373003688	chr14:104993315-104993316	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs559624119	chr14:104993322-104993323	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs375139847	chr14:104993327-104993328	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs528753877	chr14:104993332-104993333	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs371843096	chr14:104993338-104993339	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577187322	chr14:104993341-104993342	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs542426869	chr14:104993344-104993345	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs370418743	chr14:104993345-104993346	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs531064532	chr14:104993348-104993349	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs386781042	chr14:104993350-104993351	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs386781043	chr14:104993351-104993352	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs376897319	chr14:104993352-104993353	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs55963081	chr14:104993354-104993355	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs386781044	chr14:104993355-104993356	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs111164375	chr14:104993356-104993357	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs386781045	chr14:104993359-104993360	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104993000-104993200	Enhancers	Gastric	stomach
2	chr14:104993000-104993800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:104993000-104994200	ZNF genes & repeats	Fetal Brain Male	brain
4	chr14:104993200-104993400	Active TSS	Fetal Heart	heart
5	chr14:104993200-104994000	ZNF genes & repeats	Fetal Kidney	kidney
6	chr14:104993400-104994000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:104993400-104998000	Weak transcription	Fetal Heart	heart
8	chr14:104994800-104995000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr14:104997200-104997400	Enhancers	Fetal Brain Female	brain
10	chr14:104997200-104998600	Enhancers	Right Ventricle	heart
11	chr14:104997400-105000400	Weak transcription	Fetal Brain Female	brain
12	chr14:104997600-104997800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr14:104997800-104998000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr14:104997800-104998600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:104998000-104998600	Enhancers	Fetal Brain Male	brain
16	chr14:104998000-104998600	Enhancers	Fetal Heart	heart
17	chr14:104998000-104998600	Enhancers	Left Ventricle	heart
18	chr14:104998000-104998800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:104998200-104998600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr14:104998400-104998800	Enhancers	NHEK	skin
21	chr14:104998400-104999000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:104998400-104999200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:104998600-105003200	Weak transcription	Left Ventricle	heart
24	chr14:104998600-105003600	Weak transcription	Right Ventricle	heart
25	chr14:104998800-105003600	Weak transcription	NHEK	skin
26	chr14:104999000-105003600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:104999200-105003200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:104999800-105001200	Enhancers	Fetal Brain Male	brain
29	chr14:105000400-105000800	Enhancers	Fetal Brain Female	brain
30	chr14:105000400-105001400	Enhancers	Brain Germinal Matrix	brain
31	chr14:105003000-105004200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:105003200-105003800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr14:105003200-105003800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:105003200-105004000	Enhancers	Left Ventricle	heart
35	chr14:105003200-105004000	Enhancers	Right Atrium	heart
36	chr14:105003200-105004000	Enhancers	Spleen	Spleen
37	chr14:105003200-105004200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr14:105003200-105004400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr14:105003400-105004000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr14:105003400-105004000	Enhancers	Esophagus	oesophagus
41	chr14:105003400-105004000	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr14:105003400-105004000	Active TSS	Gastric	stomach
43	chr14:105003400-105004000	Enhancers	Lung	lung
44	chr14:105003600-105004000	Enhancers	Fetal Stomach	stomach
45	chr14:105003600-105004000	Enhancers	Right Ventricle	heart
46	chr14:105003600-105004200	Bivalent Enhancer	A549	lung
47	chr14:105003600-105004400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:105003600-105004400	Enhancers	NHEK	skin
49	chr14:105003800-105004200	Enhancers	HMEC	breast
50	chr14:105003800-105004400	Enhancers	Primary T helper cells PMA-I stimulated	--

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