Variant report

Variant	esv3511134
Chromosome Location	chr4:26954754-26958552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 118 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:118 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186125746	chr4:26954772-26954773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs137884333	chr4:26954787-26954788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537284608	chr4:26954845-26954846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557177602	chr4:26954850-26954851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141764936	chr4:26954864-26954865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536316597	chr4:26954871-26954872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552708885	chr4:26954939-26954940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370779070	chr4:26954955-26954956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190997597	chr4:26954966-26954967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545297852	chr4:26954988-26954989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558868282	chr4:26955007-26955008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182876703	chr4:26955013-26955014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150171312	chr4:26955021-26955022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561507418	chr4:26955029-26955030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188532190	chr4:26955031-26955032	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540684903	chr4:26955042-26955043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138573151	chr4:26955043-26955044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532599058	chr4:26955050-26955051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552597758	chr4:26955070-26955071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543102964	chr4:26955071-26955072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149305152	chr4:26955096-26955097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530804319	chr4:26955100-26955101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191910186	chr4:26955233-26955234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147479489	chr4:26955294-26955295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535974030	chr4:26955313-26955314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552983926	chr4:26955371-26955372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79520039	chr4:26955403-26955404	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs538285771	chr4:26955417-26955418	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs558111735	chr4:26955419-26955420	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs556685279	chr4:26955449-26955450	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs539443076	chr4:26955559-26955560	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs576656024	chr4:26955582-26955583	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs545593227	chr4:26955612-26955613	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs116000198	chr4:26955624-26955625	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs140024863	chr4:26955658-26955659	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs554876081	chr4:26955738-26955739	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574931665	chr4:26955779-26955780	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs540469636	chr4:26955816-26955817	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs565369962	chr4:26955829-26955830	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs560677803	chr4:26955882-26955883	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs182777461	chr4:26955885-26955886	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs546247880	chr4:26955886-26955887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs531208838	chr4:26955903-26955904	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs527949479	chr4:26955918-26955919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs530842484	chr4:26955991-26955992	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs546886956	chr4:26955995-26955996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566772189	chr4:26955999-26956000	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs550810794	chr4:26956043-26956044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs560927819	chr4:26956050-26956051	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs188342812	chr4:26956051-26956052	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26911600-26965800	Weak transcription	HMEC	breast
2	chr4:26923200-26965800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:26923200-26977200	Weak transcription	Thymus	Thymus
4	chr4:26923400-26960600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr4:26924400-26955200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr4:26938600-26969000	Weak transcription	Gastric	stomach
7	chr4:26938800-26965600	Weak transcription	NHLF	lung
8	chr4:26939200-26969000	Weak transcription	Pancreas	Pancrea
9	chr4:26942000-26961000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr4:26943200-26955000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr4:26944400-26965600	Weak transcription	Brain Anterior Caudate	brain
12	chr4:26945200-26956800	Weak transcription	Brain Angular Gyrus	brain
13	chr4:26949200-26965600	Weak transcription	NH-A	brain
14	chr4:26949400-26963400	Weak transcription	Lung	lung
15	chr4:26950000-26980200	Weak transcription	Spleen	Spleen
16	chr4:26950200-26979400	Weak transcription	Ovary	ovary
17	chr4:26950400-26959600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr4:26951800-26960200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr4:26952400-26958800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr4:26952400-26959200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr4:26952600-26955000	Weak transcription	Primary B cells from peripheral blood	blood
22	chr4:26952600-26955400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr4:26952600-26965600	Weak transcription	Psoas Muscle	Psoas
24	chr4:26952800-26955200	Weak transcription	Primary B cells from cord blood	blood
25	chr4:26952800-26956400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr4:26952800-26963400	Weak transcription	Fetal Muscle Leg	muscle
27	chr4:26953200-26961400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:26953600-26954800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr4:26954000-26954800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr4:26954000-26958800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr4:26954400-26954800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr4:26954400-26955400	Enhancers	HSMM	muscle
33	chr4:26954600-26955600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:26954600-26955800	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr4:26954600-26956000	Enhancers	Primary T cells from cord blood	blood
36	chr4:26954600-26956400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr4:26954800-26955200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr4:26954800-26955600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:26954800-26955600	Enhancers	Osteobl	bone
40	chr4:26954800-26955800	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr4:26954800-26956600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr4:26955000-26955400	Enhancers	GM12878-XiMat	blood
43	chr4:26955000-26955600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:26955000-26955600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr4:26955000-26955800	Enhancers	Primary B cells from peripheral blood	blood
46	chr4:26955000-26956000	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr4:26955200-26955400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr4:26955200-26955400	Enhancers	HSMMtube	muscle
49	chr4:26955200-26955600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr4:26955200-26955600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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