Variant report

Variant	esv1005158
Chromosome Location	chr12:528651-531441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 188 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:188 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112142960	chr12:528652-528653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10774177	chr12:528666-528667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150371159	chr12:528671-528672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61919600	chr12:528697-528698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372893007	chr12:528699-528700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10848949	chr12:528717-528718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374130794	chr12:528724-528725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12810566	chr12:528725-528726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4544060	chr12:528739-528740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377734558	chr12:528772-528773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11062879	chr12:528776-528777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529799876	chr12:528778-528779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11062880	chr12:528791-528792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11062881	chr12:528799-528800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10848950	chr12:528813-528814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548298034	chr12:528816-528817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs72187328	chr12:528818-528819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76800810	chr12:528850-528851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11062883	chr12:528865-528866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12830871	chr12:528873-528874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71293147	chr12:528887-528888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201895100	chr12:528892-528893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56167508	chr12:528899-528900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550817047	chr12:528920-528921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569729197	chr12:528942-528943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537047386	chr12:528947-528948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59173601	chr12:528961-528962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558559929	chr12:528963-528964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570775616	chr12:528965-528966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534903480	chr12:528967-528968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11327099	chr12:528997-528998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs59732872	chr12:528998-528999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs56814636	chr12:529072-529073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs57255337	chr12:529087-529088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60481953	chr12:529095-529096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56970210	chr12:529109-529110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543494563	chr12:529122-529123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59393184	chr12:529143-529144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77713796	chr12:529146-529147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs67105960	chr12:529161-529162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78288876	chr12:529169-529170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs58345465	chr12:529183-529184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71293146	chr12:529214-529215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368353141	chr12:529216-529217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71293145	chr12:529234-529235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs56391072	chr12:529237-529238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61919601	chr12:529242-529243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186786678	chr12:529256-529257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368063268	chr12:529289-529290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570145285	chr12:529290-529291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Autism	22495309	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Pleomorphic liposarcoma	18784837	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:511600-544600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr12:512000-545800	Weak transcription	HMEC	breast
3	chr12:512000-549600	Weak transcription	Colon Smooth Muscle	Colon
4	chr12:512200-540200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:512200-557800	Weak transcription	Fetal Heart	heart
6	chr12:512600-528800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:512600-552200	Weak transcription	Fetal Brain Male	brain
8	chr12:513600-529000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:513600-529800	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:514200-528800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr12:514400-528800	Strong transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:518400-528800	Strong transcription	Dnd41	blood
13	chr12:518800-529800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr12:519400-529800	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:519800-528800	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr12:519800-528800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:522000-534400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr12:522000-541800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:522000-541800	Weak transcription	Pancreas	Pancrea
20	chr12:522000-542000	Weak transcription	HSMMtube	muscle
21	chr12:522000-551800	Weak transcription	NHEK	skin
22	chr12:524400-532400	Weak transcription	K562	blood
23	chr12:524400-534400	Weak transcription	Esophagus	oesophagus
24	chr12:524400-541000	Weak transcription	NH-A	brain
25	chr12:524400-541200	Weak transcription	HUVEC	blood vessel
26	chr12:524400-542400	Weak transcription	NHLF	lung
27	chr12:524400-549800	Weak transcription	NHDF-Ad	bronchial
28	chr12:524400-550600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr12:524400-553600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr12:524400-556800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:525400-532800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:525800-528800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr12:525800-528800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr12:525800-528800	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr12:525800-529800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr12:526200-557800	Weak transcription	Stomach Mucosa	stomach
37	chr12:526400-528800	Strong transcription	Adipose Nuclei	Adipose
38	chr12:526400-528800	Strong transcription	Fetal Brain Female	brain
39	chr12:526400-528800	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr12:526400-545600	Weak transcription	Psoas Muscle	Psoas
41	chr12:526600-528800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:526600-541000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr12:526800-534400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr12:527600-528800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
45	chr12:527600-529000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:527800-528800	Strong transcription	Skeletal Muscle Male	skeletal muscle
47	chr12:528000-552600	Weak transcription	Osteobl	bone
48	chr12:528200-532800	Weak transcription	Fetal Intestine Small	intestine
49	chr12:528200-533400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr12:528200-534200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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