Variant report

Variant	nsv1022118
Chromosome Location	chr7:19178075-19518160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:19444572-19445053	A549	lung:	n/a	n/a
2	ATF3	chr7:19401699-19402094	HCT-116	colon:	n/a	n/a
3	ATF3	chr7:19444493-19444867	A549	lung:	n/a	n/a
4	BACH1	chr7:19347264-19347555	K562	blood:	n/a	chr7:19347366-19347380
5	BACH1	chr7:19347073-19347532	H1-hESC	embryonic stem cell:	n/a	chr7:19347366-19347380
6	BCL3	chr7:19444394-19444990	A549	lung:	n/a	chr7:19444641-19444650
7	BHLHE40	chr7:19422585-19422633	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:19437440-19437816	GM12878	blood:	n/a	n/a
9	CBX3	chr7:19444505-19444941	HCT-116	colon:	n/a	n/a
10	CEBPB	chr7:19334183-19334506	HepG2	liver:	n/a	chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360 chr7:19334351-19334360 chr7:19334350-19334361 chr7:19334351-19334360 chr7:19334349-19334362 chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360
11	CEBPB	chr7:19291279-19291589	K562	blood:	n/a	chr7:19291449-19291458 chr7:19291448-19291459 chr7:19291449-19291458 chr7:19291447-19291458 chr7:19291449-19291458 chr7:19291449-19291458
12	CEBPB	chr7:19187024-19187260	H1-hESC	embryonic stem cell:	n/a	chr7:19187110-19187123 chr7:19187111-19187122 chr7:19187110-19187123
13	CEBPB	chr7:19291368-19291588	A549	lung:	n/a	chr7:19291449-19291458 chr7:19291448-19291459 chr7:19291449-19291458 chr7:19291447-19291458 chr7:19291449-19291458 chr7:19291449-19291458
14	CEBPB	chr7:19324206-19324791	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:19297107-19297325	HepG2	liver:	n/a	chr7:19297180-19297191
16	CEBPB	chr7:19477072-19477270	IMR90	lung:	n/a	n/a
17	CEBPB	chr7:19295359-19295597	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:19187004-19187204	A549	lung:	n/a	chr7:19187110-19187123 chr7:19187111-19187122 chr7:19187110-19187123
19	CEBPB	chr7:19334172-19334510	ECC-1	luminal epithelium:	n/a	chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360 chr7:19334351-19334360 chr7:19334350-19334361 chr7:19334351-19334360 chr7:19334349-19334362 chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360
20	CEBPB	chr7:19316088-19316408	HepG2	liver:	n/a	chr7:19316254-19316265
21	CEBPB	chr7:19445196-19445500	A549	lung:	n/a	chr7:19445336-19445347
22	CEBPB	chr7:19308350-19308919	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:19379927-19380128	A549	lung:	n/a	n/a
24	CEBPB	chr7:19379888-19380200	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:19406922-19407130	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:19308340-19308598	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:19186943-19187269	IMR90	lung:	n/a	chr7:19187110-19187123 chr7:19187111-19187122 chr7:19187110-19187123
28	CEBPB	chr7:19444429-19445027	HCT-116	colon:	n/a	n/a
29	CEBPB	chr7:19444478-19444920	A549	lung:	n/a	n/a
30	CEBPB	chr7:19368409-19368599	HepG2	liver:	n/a	chr7:19368529-19368542 chr7:19368530-19368541 chr7:19368529-19368540
31	CEBPB	chr7:19334178-19334535	A549	lung:	n/a	chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360 chr7:19334351-19334360 chr7:19334350-19334361 chr7:19334351-19334360 chr7:19334349-19334362 chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360
32	CEBPB	chr7:19401780-19402111	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:19334186-19334532	IMR90	lung:	n/a	chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360 chr7:19334351-19334360 chr7:19334350-19334361 chr7:19334351-19334360 chr7:19334349-19334362 chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360
34	CEBPB	chr7:19334241-19334479	Hela-S3	cervix:	n/a	chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360 chr7:19334351-19334360 chr7:19334350-19334361 chr7:19334351-19334360 chr7:19334349-19334362 chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360
35	CEBPB	chr7:19316101-19316387	IMR90	lung:	n/a	chr7:19316254-19316265
36	CEBPB	chr7:19444492-19445539	IMR90	lung:	n/a	chr7:19445336-19445347
37	CEBPB	chr7:19295352-19295559	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:19263326-19263572	IMR90	lung:	n/a	chr7:19263419-19263430
39	CEBPB	chr7:19509394-19509590	A549	lung:	n/a	chr7:19509476-19509487
40	CEBPB	chr7:19431952-19432321	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:19508896-19509126	HepG2	liver:	n/a	chr7:19508982-19508993 chr7:19508983-19508994 chr7:19508982-19508993 chr7:19508982-19508995
42	CEBPB	chr7:19444404-19445628	A549	lung:	n/a	chr7:19445336-19445347
43	CEBPB	chr7:19187041-19187190	K562	blood:	n/a	chr7:19187110-19187123 chr7:19187111-19187122 chr7:19187110-19187123
44	CEBPB	chr7:19509353-19509598	HepG2	liver:	n/a	chr7:19509476-19509487
45	CEBPB	chr7:19291345-19291589	Hela-S3	cervix:	n/a	chr7:19291449-19291458 chr7:19291448-19291459 chr7:19291449-19291458 chr7:19291447-19291458 chr7:19291449-19291458 chr7:19291449-19291458
46	CEBPB	chr7:19446082-19446303	A549	lung:	n/a	n/a
47	CEBPB	chr7:19263306-19263565	HepG2	liver:	n/a	chr7:19263419-19263430
48	CEBPB	chr7:19334197-19334469	ECC-1	luminal epithelium:	n/a	chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360 chr7:19334351-19334360 chr7:19334350-19334361 chr7:19334351-19334360 chr7:19334349-19334362 chr7:19334349-19334362 chr7:19334351-19334360 chr7:19334349-19334360
49	CEBPB	chr7:19291290-19291619	HepG2	liver:	n/a	chr7:19291449-19291458 chr7:19291448-19291459 chr7:19291449-19291458 chr7:19291447-19291458 chr7:19291449-19291458 chr7:19291449-19291458
50	CEBPB	chr7:19444511-19445576	Hela-S3	cervix:	n/a	chr7:19445336-19445347

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19185260-19185310	SAEC	small airway:	n/a
2	chr7:19185260-19185310	SAEC	small airway:	n/a
3	chr7:19183753-19183803	HCT-116	colon:	n/a
4	chr7:19184427-19184477	MCF10A-Er-Src	breast:	n/a
5	chr7:19185139-19185189	T-47D	breast:	n/a
6	chr7:19183753-19183803	AoSMC	blood vessel:	n/a
7	chr7:19183563-19183613	HAEpiC	amniotic membrane:	n/a
8	chr7:19184427-19184477	ovcar-3	ovarian:	n/a
9	chr7:19184555-19184605	AG09309	skin:	n/a
10	chr7:19417585-19417635	HMEC	breast:	n/a
11	chr7:19417585-19417635	PFSK-1	brain:	n/a
12	chr7:19182017-19182067	HUVEC	blood vessel:	n/a
13	chr7:19184950-19185000	SK-N-SH	brain:	n/a
14	chr7:19185139-19185189	HEEpiC	esophagus:	n/a
15	chr7:19182334-19182384	Hepatocyte	liver:	n/a
16	chr7:19185165-19185215	Hepatocyte	liver:	n/a
17	chr7:19443825-19443875	Hela-S3	cervix:	n/a
18	chr7:19185165-19185215	CMK	blood:	n/a
19	chr7:19184273-19184323	CMK	blood:	n/a
20	chr7:19185165-19185215	HUVEC	blood vessel:	n/a
21	chr7:19184555-19184605	AG04449	skin:	fetal
22	chr7:19185139-19185189	SKMC	muscle:	n/a
23	chr7:19184427-19184477	Hepatocyte	liver:	n/a
24	chr7:19183325-19183375	HIPEpiC	eye:	n/a
25	chr7:19209204-19209254	GM12892	blood:	n/a
26	chr7:19183325-19183375	HMEC	breast:	n/a
27	chr7:19408343-19408393	HEK293	kidney:	embryo
28	chr7:19183325-19183375	GM19239	blood:	n/a
29	chr7:19209204-19209254	H1-hESC	embryonic stem cell:	embryo
30	chr7:19185139-19185189	ProgFib	skin:	n/a
31	chr7:19453933-19453983	HEK293	kidney:	embryo
32	chr7:19185139-19185189	SK-N-SH	brain:	n/a
33	chr7:19183563-19183613	HepG2	liver:	n/a
34	chr7:19182334-19182384	SAEC	small airway:	n/a
35	chr7:19184961-19185011	GM12891	blood:	n/a
36	chr7:19185165-19185215	SKMC	muscle:	n/a
37	chr7:19184950-19185000	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:19443825-19443875	PrEC	prostate:	n/a
39	chr7:19183325-19183375	AG09319	gingival:	n/a
40	chr7:19183563-19183613	Hepatocyte	liver:	n/a
41	chr7:19184427-19184477	AG04450	lung:	fetal
42	chr7:19453933-19453983	SAEC	small airway:	n/a
43	chr7:19184555-19184605	SK-N-SH_RA	brain:	n/a
44	chr7:19183231-19183281	ovcar-3	ovarian:	n/a
45	chr7:19184950-19185000	PANC-1	pancreas:	n/a
46	chr7:19185260-19185310	A549	lung:	n/a
47	chr7:19183732-19183782	SK-N-MC	brain:	n/a
48	chr7:19183563-19183613	HEEpiC	esophagus:	n/a
49	chr7:19417585-19417635	U87	brain:	n/a
50	chr7:19184273-19184323	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:19329990..19331795-chr7:19331809..19334406,3	K562	blood:
2	chr7:19205244..19207935-chr7:19216536..19218730,2	K562	blood:
3	chr7:19502491..19504536-chr7:19508124..19510768,2	K562	blood:
4	chr7:19198266..19200547-chr7:19202744..19204573,2	K562	blood:
5	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
6	chr7:19205244..19207935-chr7:19216536..19218730,2	K562	blood:
7	chr7:19164726..19167634-chr7:19176686..19178206,2	K562	blood:
8	chr7:19502491..19504536-chr7:19508124..19510768,2	K562	blood:
9	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:
10	chr7:19400460..19402875-chr7:19412134..19413923,2	K562	blood:
11	chr7:19429082..19431210-chr7:19440295..19442664,2	K562	blood:
12	chr7:19244268..19246835-chr7:19247429..19249868,2	K562	blood:
13	chr7:19198266..19200547-chr7:19202744..19204573,2	K562	blood:
14	chr7:19244268..19246835-chr7:19247429..19249868,2	K562	blood:
15	chr7:19329990..19331795-chr7:19331809..19334406,3	K562	blood:
16	chr14:53017346..53020314-chr7:19356752..19358807,2	MCF-7	breast:
17	chr7:19161356..19162289-chr7:19481424..19482541,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-5	chr7:19444955-19444993	ENSG00000223838
2	lnc-HDAC9-12	chr7:19411480-19411518	NONHSAT119386
3	lnc-HDAC9-5	chr7:19394363-19394508	ENSG00000223838
4	lnc-HDAC9-5	chr7:19443324-19443386	ENSG00000223838
5	lnc-HDAC9-12	chr7:19360888-19361033	NONHSAT119386
6	lnc-HDAC9-12	chr7:19359682-19359789	NONHSAT119386
7	lnc-HDAC9-12	chr7:19409849-19409911	NONHSAT119386
8	lnc-HDAC9-5	chr7:19393157-19393264	ENSG00000223838

Variant related genes	Relation type
ENSG00000223838	TF binding region
ENSG00000229533	TF binding region
FERD3L	TF binding region
ENSG00000223838	CpG island
ENSG00000229533	CpG island
FERD3L	CpG island
ENSG00000087301	chromatin interactions
ENSG00000180998	chromatin interactions

Extended variants
information (count: 8096 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:8096 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578066513	chr7:19178205-19178206	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs150171823	chr7:19178241-19178242	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs183486051	chr7:19178247-19178248	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs560753749	chr7:19178254-19178255	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs527956764	chr7:19178265-19178266	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs75753696	chr7:19178275-19178276	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs138575176	chr7:19178311-19178312	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs149298989	chr7:19178354-19178355	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11979718	chr7:19178542-19178543	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs377758674	chr7:19178582-19178583	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs78492099	chr7:19179257-19179258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs75599163	chr7:19179263-19179264	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs79180391	chr7:19179311-19179312	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs547090069	chr7:19179312-19179313	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs373183381	chr7:19179321-19179322	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs113353588	chr7:19179410-19179411	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs565292846	chr7:19179417-19179418	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529697225	chr7:19179439-19179440	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532649793	chr7:19179442-19179443	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs35048040	chr7:19179492-19179493	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548461335	chr7:19179520-19179521	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs574796101	chr7:19179543-19179544	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs111230116	chr7:19179574-19179575	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs537233270	chr7:19179592-19179593	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs143810064	chr7:19179602-19179603	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs535738114	chr7:19179620-19179621	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs562713132	chr7:19179627-19179628	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs147253813	chr7:19179636-19179637	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs78803669	chr7:19179677-19179678	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs572464230	chr7:19179723-19179724	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542704033	chr7:19179724-19179725	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs555223910	chr7:19179739-19179740	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs185355148	chr7:19179741-19179742	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs548707043	chr7:19179779-19179780	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs544114461	chr7:19179804-19179805	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs80352452	chr7:19179825-19179826	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs557668342	chr7:19179843-19179844	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532573481	chr7:19179859-19179860	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79038426	chr7:19179868-19179869	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs367869751	chr7:19179876-19179877	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117545517	chr7:19179924-19179925	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558839418	chr7:19179938-19179939	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547910343	chr7:19179949-19179950	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563312601	chr7:19179989-19179990	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552504199	chr7:19180174-19180175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs570620043	chr7:19180178-19180179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs181299892	chr7:19180179-19180180	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547911477	chr7:19180271-19180272	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs566208028	chr7:19180281-19180282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs140726920	chr7:19180297-19180298	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myelofibrosis	22110671	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19178200-19178600	Active TSS	Osteobl	bone
2	chr7:19179400-19179600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:19179400-19180000	Enhancers	HSMM	muscle
4	chr7:19179400-19180000	Enhancers	HSMMtube	muscle
5	chr7:19179800-19180000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
6	chr7:19182800-19183200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr7:19183000-19183200	Weak transcription	Pancreas	Pancrea
8	chr7:19183000-19183400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
9	chr7:19183000-19183600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
10	chr7:19183000-19183800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
11	chr7:19183000-19185000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
12	chr7:19183000-19185000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr7:19183000-19185000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
14	chr7:19183000-19185400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
15	chr7:19183200-19183400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
16	chr7:19183200-19183400	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr7:19183200-19183400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:19183200-19183400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
19	chr7:19183200-19183400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:19183200-19183400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:19183200-19183400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
22	chr7:19183200-19183600	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:19183200-19183600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
24	chr7:19183200-19183600	Bivalent Enhancer	Brain Germinal Matrix	brain
25	chr7:19183200-19183600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
26	chr7:19183200-19183800	Bivalent Enhancer	Fetal Stomach	stomach
27	chr7:19183200-19183800	Enhancers	Gastric	stomach
28	chr7:19183200-19185000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:19183200-19185000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:19183200-19185000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:19183200-19185000	Enhancers	Pancreas	Pancrea
32	chr7:19183200-19185200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr7:19183200-19185200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr7:19183200-19185600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:19183400-19183600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
36	chr7:19183400-19183600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:19183400-19183600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:19183400-19183600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:19183400-19183600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr7:19183400-19183600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:19183400-19183600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:19183400-19183600	Bivalent Enhancer	Left Ventricle	heart
43	chr7:19183400-19183600	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
44	chr7:19183400-19183600	Flanking Active TSS	Spleen	Spleen
45	chr7:19183400-19183800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:19183400-19183800	Flanking Active TSS	Right Ventricle	heart
47	chr7:19183400-19184000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
48	chr7:19183400-19184000	Bivalent Enhancer	Lung	lung
49	chr7:19183400-19184400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:19183400-19184400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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