Variant report

Variant	esv3495213
Chromosome Location	chr8:131060520-131063568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:131062555..131064822-chr8:131096828..131099567,2	K562	blood:
2	chr8:131056726..131059122-chr8:131059475..131061608,2	K562	blood:

Extended variants
information (count: 208 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:208 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143134730	chr8:131060548-131060549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551123215	chr8:131060578-131060579	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569520816	chr8:131060587-131060588	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147448516	chr8:131060591-131060592	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201861591	chr8:131060613-131060614	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111390047	chr8:131060614-131060615	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558906708	chr8:131060623-131060624	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369353343	chr8:131060649-131060650	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573706749	chr8:131060650-131060651	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375927457	chr8:131060670-131060671	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73712851	chr8:131060673-131060674	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113688858	chr8:131060674-131060675	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116902591	chr8:131060710-131060711	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537512358	chr8:131060716-131060717	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578152754	chr8:131060721-131060722	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545685758	chr8:131060770-131060771	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139883483	chr8:131060785-131060786	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553108360	chr8:131060786-131060787	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575926400	chr8:131060835-131060836	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs543279610	chr8:131060854-131060855	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs561348083	chr8:131060873-131060874	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs182082239	chr8:131060937-131060938	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs186420072	chr8:131060951-131060952	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs79557073	chr8:131060952-131060953	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs533034269	chr8:131061007-131061008	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114446819	chr8:131061035-131061036	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569645968	chr8:131061065-131061066	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191173673	chr8:131061089-131061090	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199538527	chr8:131061136-131061137	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567238216	chr8:131061159-131061160	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117278781	chr8:131061162-131061163	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201891607	chr8:131061241-131061242	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141761681	chr8:131061243-131061244	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577588274	chr8:131061246-131061247	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539304744	chr8:131061250-131061251	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200370629	chr8:131061261-131061262	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577208099	chr8:131061283-131061284	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557671344	chr8:131061320-131061321	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201943007	chr8:131061333-131061334	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576036151	chr8:131061388-131061389	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200289499	chr8:131061389-131061390	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543241142	chr8:131061390-131061391	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180793169	chr8:131061399-131061400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186658495	chr8:131061401-131061402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs5895022	chr8:131061410-131061411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540726797	chr8:131061412-131061413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199586324	chr8:131061431-131061432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373575932	chr8:131061433-131061434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528779397	chr8:131061449-131061450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191011540	chr8:131061454-131061455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131041400-131068600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:131051800-131063800	Weak transcription	Aorta	Aorta
3	chr8:131055000-131063800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:131055200-131063000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:131055400-131063800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:131055400-131064600	Weak transcription	HMEC	breast
7	chr8:131056000-131066600	Weak transcription	Hela-S3	cervix
8	chr8:131058000-131063000	Weak transcription	Fetal Intestine Large	intestine
9	chr8:131058000-131063800	Weak transcription	Pancreas	Pancrea
10	chr8:131058000-131065200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr8:131058000-131065400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:131058400-131062800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:131058400-131063600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr8:131058400-131063800	Weak transcription	Fetal Brain Male	brain
15	chr8:131058400-131064200	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:131058400-131065000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:131058400-131065000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr8:131058400-131065200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:131058400-131065400	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr8:131058400-131066400	Weak transcription	Ovary	ovary
21	chr8:131058400-131066600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:131058400-131066600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr8:131058400-131073800	Weak transcription	Stomach Mucosa	stomach
24	chr8:131058600-131060600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:131058600-131060600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr8:131058600-131066000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr8:131058600-131066600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr8:131058600-131068000	Weak transcription	Colonic Mucosa	Colon
29	chr8:131058800-131060600	Enhancers	Adipose Nuclei	Adipose
30	chr8:131058800-131062800	Weak transcription	Osteobl	bone
31	chr8:131058800-131063600	Weak transcription	Brain Anterior Caudate	brain
32	chr8:131058800-131063800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr8:131058800-131063800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:131058800-131065200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr8:131058800-131065200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr8:131058800-131066200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr8:131058800-131066400	Weak transcription	Colon Smooth Muscle	Colon
38	chr8:131058800-131066600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr8:131058800-131066800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr8:131058800-131068200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr8:131058800-131068600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr8:131058800-131068800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr8:131058800-131074200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr8:131059000-131060600	Weak transcription	Brain Hippocampus Middle	brain
45	chr8:131059000-131061200	Strong transcription	Fetal Stomach	stomach
46	chr8:131059000-131062600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr8:131059000-131063200	Weak transcription	Fetal Thymus	thymus
48	chr8:131059000-131063200	Weak transcription	NH-A	brain
49	chr8:131059000-131063800	Weak transcription	Primary hematopoietic stem cells	blood
50	chr8:131059000-131065000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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