Variant report

Variant	nsv1022489
Chromosome Location	chr8:95212660-95273564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1435)
CpG islands
(count:1099)
Chromatin interactive
region (count:39)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1435 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:95254352-95254671	HepG2	liver:	n/a	n/a
2	ATF1	chr8:95218407-95218446	K562	blood:	n/a	n/a
3	ATF1	chr8:95231164-95231381	K562	blood:	n/a	n/a
4	ATF2	chr8:95229597-95230197	GM12878	blood:	n/a	n/a
5	ATF2	chr8:95254330-95254711	GM12878	blood:	n/a	n/a
6	ATF2	chr8:95230950-95231630	GM12878	blood:	n/a	n/a
7	ATF2	chr8:95232569-95233051	GM12878	blood:	n/a	n/a
8	ATF2	chr8:95230930-95231587	GM12878	blood:	n/a	n/a
9	ATF2	chr8:95232611-95233091	GM12878	blood:	n/a	n/a
10	ATF3	chr8:95254032-95255067	A549	lung:	n/a	n/a
11	ATF3	chr8:95254069-95255177	A549	lung:	n/a	n/a
12	BACH1	chr8:95242663-95242898	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:95246430-95246771	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:95250099-95250250	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:95231967-95232122	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr8:95246603-95246925	GM12878	blood:	n/a	n/a
17	BATF	chr8:95231134-95231401	GM12878	blood:	n/a	n/a
18	BATF	chr8:95232624-95232998	GM12878	blood:	n/a	n/a
19	BATF	chr8:95254209-95254678	GM12878	blood:	n/a	chr8:95254484-95254494 chr8:95254483-95254494
20	BATF	chr8:95230966-95231514	GM12878	blood:	n/a	n/a
21	BATF	chr8:95229668-95229959	GM12878	blood:	n/a	n/a
22	BATF	chr8:95232596-95233020	GM12878	blood:	n/a	n/a
23	BATF	chr8:95254321-95254662	GM12878	blood:	n/a	chr8:95254484-95254494 chr8:95254483-95254494
24	BCL11A	chr8:95231167-95231430	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:95246739-95247197	GM12878	blood:	n/a	chr8:95247139-95247152
26	BCL11A	chr8:95232697-95233050	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:95231060-95231542	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:95221856-95222050	GM12878	blood:	n/a	chr8:95222039-95222048
29	BCL11A	chr8:95254262-95254659	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:95232740-95232973	GM12878	blood:	n/a	n/a
31	BCL3	chr8:95254275-95254702	GM12878	blood:	n/a	n/a
32	BCL3	chr8:95254107-95255151	A549	lung:	n/a	n/a
33	BCL3	chr8:95231078-95231513	GM12878	blood:	n/a	n/a
34	BCL3	chr8:95254109-95255295	A549	lung:	n/a	n/a
35	BCL3	chr8:95245622-95245855	GM12878	blood:	n/a	n/a
36	BCLAF1	chr8:95232585-95232979	GM12878	blood:	n/a	n/a
37	BCLAF1	chr8:95254316-95254694	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:95229554-95230109	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:95231000-95231623	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:95267076-95267263	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:95273316-95273398	GM12878	blood:	n/a	n/a
42	BHLHE40	chr8:95231021-95231589	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:95246449-95246560	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:95256621-95256996	K562	blood:	n/a	n/a
45	BHLHE40	chr8:95221813-95222111	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:95254280-95254636	K562	blood:	n/a	n/a
47	BHLHE40	chr8:95254342-95254658	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:95254278-95254851	HepG2	liver:	n/a	n/a
49	BRCA1	chr8:95254284-95254894	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr8:95231883-95232347	Hela-S3	cervix:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95220583-95220633	GM06990	blood:	n/a
2	chr8:95220583-95220633	GM06990	blood:	n/a
3	chr8:95220779-95220829	BE2_C	brain:	n/a
4	chr8:95246814-95246864	AG10803	skin:	n/a
5	chr8:95266905-95266955	BE2_C	brain:	n/a
6	chr8:95229525-95229575	AoSMC	blood vessel:	n/a
7	chr8:95229754-95229804	GM12878	blood:	n/a
8	chr8:95220779-95220829	ProgFib	skin:	n/a
9	chr8:95246814-95246864	Caco-2	colon:	n/a
10	chr8:95229664-95229714	SK-N-SH	brain:	n/a
11	chr8:95230984-95231034	SK-N-SH_RA	brain:	n/a
12	chr8:95246699-95246749	GM12878	blood:	n/a
13	chr8:95271635-95271685	Jurkat	blood:	n/a
14	chr8:95266905-95266955	Caco-2	colon:	n/a
15	chr8:95238935-95238985	A549	lung:	n/a
16	chr8:95220779-95220829	AG10803	skin:	n/a
17	chr8:95229754-95229804	SK-N-MC	brain:	n/a
18	chr8:95229664-95229714	BJ	skin:	n/a
19	chr8:95246699-95246749	ECC-1	luminal epithelium:	n/a
20	chr8:95246814-95246864	PFSK-1	brain:	n/a
21	chr8:95221197-95221247	GM19239	blood:	n/a
22	chr8:95271635-95271685	AG09319	gingival:	n/a
23	chr8:95271635-95271685	HCT-116	colon:	n/a
24	chr8:95254202-95254252	NHDF-neo	bronchial:	n/a
25	chr8:95221197-95221247	ProgFib	skin:	n/a
26	chr8:95229872-95229922	U87	brain:	n/a
27	chr8:95246514-95246564	SK-N-SH	brain:	n/a
28	chr8:95246699-95246749	AG10803	skin:	n/a
29	chr8:95229754-95229804	GM12892	blood:	n/a
30	chr8:95220583-95220633	H1-hESC	embryonic stem cell:	embryo
31	chr8:95230984-95231034	BE2_C	brain:	n/a
32	chr8:95254202-95254252	HEEpiC	esophagus:	n/a
33	chr8:95229664-95229714	AG09309	skin:	n/a
34	chr8:95230984-95231034	MCF10A-Er-Src	breast:	n/a
35	chr8:95229872-95229922	BE2_C	brain:	n/a
36	chr8:95229664-95229714	ECC-1	luminal epithelium:	n/a
37	chr8:95220583-95220633	AG04450	lung:	fetal
38	chr8:95220779-95220829	AG09319	gingival:	n/a
39	chr8:95220779-95220829	HL-60	blood:	n/a
40	chr8:95229754-95229804	Hela-S3	cervix:	n/a
41	chr8:95221342-95221392	NT2-D1	testis:	n/a
42	chr8:95271635-95271685	HepG2	liver:	n/a
43	chr8:95266905-95266955	HRE	kidney:	n/a
44	chr8:95221342-95221392	MCF-7	breast:	n/a
45	chr8:95246514-95246564	A549	lung:	n/a
46	chr8:95229872-95229922	HRCEpiC	kidney:	n/a
47	chr8:95221342-95221392	AG04449	skin:	fetal
48	chr8:95221197-95221247	U87	brain:	n/a
49	chr8:95221342-95221392	U87	brain:	n/a
50	chr8:95230984-95231034	K562	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95252312..95253964-chr8:95260272..95262421,3	MCF-7	breast:
2	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
3	chr8:95240844..95244152-chr8:95245097..95248087,3	MCF-7	breast:
4	chr8:95244367..95248911-chr8:95252094..95255731,6	MCF-7	breast:
5	chr8:95244367..95248911-chr8:95252094..95255731,6	MCF-7	breast:
6	chr8:95256075..95257959-chr8:95283640..95285924,2	K562	blood:
7	chr8:95240844..95244152-chr8:95245097..95248087,3	MCF-7	breast:
8	chr8:95252636..95255137-chr8:95271154..95272846,2	MCF-7	breast:
9	chr8:95259315..95260909-chr8:95269095..95271460,2	MCF-7	breast:
10	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
11	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
12	chr8:95263857..95265470-chr8:95267384..95270034,2	MCF-7	breast:
13	chr20:52281172..52282725-chr8:95268610..95270828,2	MCF-7	breast:
14	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
15	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
16	chr8:95259315..95260909-chr8:95269095..95271460,2	MCF-7	breast:
17	chr8:95218436..95218963-chr8:95284617..95285220,2	MCF-7	breast:
18	chr8:95242861..95244943-chr8:95255431..95257356,2	MCF-7	breast:
19	chr8:95252636..95255137-chr8:95271154..95272846,2	MCF-7	breast:
20	chr8:95219101..95220726-chr8:95272538..95274563,2	MCF-7	breast:
21	chr8:95263857..95265470-chr8:95267384..95270034,2	MCF-7	breast:
22	chr8:95246301..95247205-chr9:108320150..108320809,2	HCT-116	colon:
23	chr8:95253573..95256395-chr8:95272971..95276826,4	MCF-7	breast:
24	chr8:95216472..95218639-chr8:95229347..95231439,2	MCF-7	breast:
25	chr8:95264526..95268344-chr8:95270194..95275198,8	MCF-7	breast:
26	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
27	chr8:95252911..95255194-chr8:95273270..95275304,2	MCF-7	breast:
28	chr8:95259639..95261936-chr8:95271778..95274388,2	MCF-7	breast:
29	chr8:95215544..95217656-chr8:95220305..95222366,3	MCF-7	breast:
30	chr8:95265284..95269210-chr8:95271122..95274940,6	MCF-7	breast:
31	chr8:95228655..95231086-chr8:95245435..95247101,2	MCF-7	breast:
32	chr8:95238887..95240526-chr8:95244307..95246160,2	MCF-7	breast:
33	chr8:95224589..95225412-chr8:95369113..95370095,2	MCF-7	breast:
34	chr8:95217922..95218880-chr8:95369574..95370256,2	MCF-7	breast:
35	chr8:95238887..95240526-chr8:95244307..95246160,2	MCF-7	breast:
36	chr8:95254047..95254705-chr8:95369510..95370184,2	K562	blood:
37	chr8:95252312..95253964-chr8:95260272..95262421,3	MCF-7	breast:
38	chr8:95242861..95244943-chr8:95255431..95257356,2	MCF-7	breast:
39	chr8:95176962..95177482-chr8:95225796..95226601,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GEM-1	chr8:95214141-95214393	NONHSAT127766
2	lnc-GEM-1	chr8:95214701-95215280	NONHSAT127766

No data

Variant related genes	Relation type
CDH17	TF binding region
GEM	TF binding region
ENSG00000249510	TF binding region
CDH17	CpG island
GEM	CpG island
ENSG00000249510	CpG island
ENSG00000106692	chromatin interactions
ENSG00000228317	chromatin interactions
ENSG00000079112	chromatin interactions
ENSG00000164949	chromatin interactions

Extended variants
information (count: 2442 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2442 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575135536	chr8:95212698-95212699	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552817996	chr8:95212700-95212701	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573215588	chr8:95212708-95212709	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs4735275	chr8:95212742-95212743	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs568720538	chr8:95212765-95212766	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2446864	chr8:95212776-95212777	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150911149	chr8:95212780-95212781	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2446863	chr8:95212784-95212785	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75492183	chr8:95212791-95212792	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10600702	chr8:95212795-95212796	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368576539	chr8:95212798-95212799	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112405966	chr8:95212802-95212803	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192741808	chr8:95212848-95212849	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148347148	chr8:95212858-95212859	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113080616	chr8:95212889-95212890	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs57686136	chr8:95212894-95212895	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58086614	chr8:95212914-95212915	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377605109	chr8:95212916-95212917	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183309466	chr8:95212944-95212945	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs59960318	chr8:95212984-95212985	Weak transcription Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564680809	chr8:95213009-95213010	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533532418	chr8:95213023-95213024	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547339664	chr8:95213030-95213031	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567032913	chr8:95213055-95213056	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528126133	chr8:95213069-95213070	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142291438	chr8:95213077-95213078	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77415900	chr8:95213078-95213079	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11775940	chr8:95213119-95213120	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111594860	chr8:95213258-95213259	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556949917	chr8:95213316-95213317	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371870101	chr8:95213329-95213330	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536752411	chr8:95213330-95213331	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2340034	chr8:95213331-95213332	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557670845	chr8:95213379-95213380	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556602334	chr8:95213395-95213396	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146393456	chr8:95213444-95213445	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539221948	chr8:95213475-95213476	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139816225	chr8:95213496-95213497	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143124818	chr8:95213555-95213556	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535890096	chr8:95213567-95213568	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375699791	chr8:95213574-95213575	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555478570	chr8:95213600-95213601	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577487701	chr8:95213603-95213604	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543329545	chr8:95213613-95213614	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150750323	chr8:95213625-95213626	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544940527	chr8:95213672-95213673	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139106576	chr8:95213676-95213677	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188088901	chr8:95213688-95213689	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375272254	chr8:95213699-95213700	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540814354	chr8:95213703-95213704	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1504 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95207400-95213400	Enhancers	Fetal Intestine Large	intestine
2	chr8:95210800-95213000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr8:95211200-95213800	Enhancers	A549	lung
4	chr8:95211600-95214400	Genic enhancers	Fetal Intestine Small	intestine
5	chr8:95212000-95213000	Enhancers	Small Intestine	intestine
6	chr8:95212200-95218000	Weak transcription	Colonic Mucosa	Colon
7	chr8:95212400-95213600	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr8:95212400-95217000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:95212600-95213000	Active TSS	Duodenum Mucosa	Duodenum
10	chr8:95212600-95220600	Weak transcription	Stomach Mucosa	stomach
11	chr8:95212800-95213400	Enhancers	K562	blood
12	chr8:95213000-95214400	Enhancers	Duodenum Mucosa	Duodenum
13	chr8:95213000-95214800	Weak transcription	Small Intestine	intestine
14	chr8:95213000-95215800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr8:95213400-95213800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr8:95213400-95214000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr8:95213400-95214200	Genic enhancers	Fetal Intestine Large	intestine
18	chr8:95213600-95214200	Genic enhancers	Rectal Mucosa Donor 29	rectum
19	chr8:95213800-95214800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr8:95213800-95218000	Weak transcription	A549	lung
21	chr8:95214200-95215200	Strong transcription	Fetal Intestine Large	intestine
22	chr8:95214200-95215200	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr8:95214400-95215200	Strong transcription	Fetal Intestine Small	intestine
24	chr8:95214400-95215600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:95214800-95215200	Enhancers	Small Intestine	intestine
26	chr8:95214800-95216200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr8:95215000-95215800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr8:95215200-95215400	Genic enhancers	Fetal Intestine Large	intestine
29	chr8:95215200-95216400	Weak transcription	Fetal Intestine Small	intestine
30	chr8:95215200-95217000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr8:95215200-95220000	Weak transcription	Small Intestine	intestine
32	chr8:95215400-95217000	Weak transcription	Fetal Intestine Large	intestine
33	chr8:95215600-95216000	Active TSS	Duodenum Mucosa	Duodenum
34	chr8:95215800-95216200	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr8:95215800-95220000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:95216000-95217200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr8:95216200-95217000	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr8:95216400-95217400	Genic enhancers	Fetal Intestine Small	intestine
39	chr8:95217000-95217200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr8:95217000-95217200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr8:95217000-95218000	Enhancers	Fetal Intestine Large	intestine
42	chr8:95217000-95218000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr8:95217200-95217400	Active TSS	Rectal Mucosa Donor 29	rectum
44	chr8:95217200-95219600	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr8:95217200-95221400	Active TSS	Duodenum Mucosa	Duodenum
46	chr8:95217400-95217600	Enhancers	Fetal Intestine Small	intestine
47	chr8:95217400-95217800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
48	chr8:95217600-95218000	Flanking Active TSS	Fetal Intestine Small	intestine
49	chr8:95217600-95220200	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr8:95217800-95218000	Active TSS	Rectal Mucosa Donor 29	rectum

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