Variant report

Variant	esv3516146
Chromosome Location	chr7:53099945-53356180
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	BACH1	chr7:53286655-53287303	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:53233835-53234042	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:53118189-53118465	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:53221229-53221402	GM12878	blood:	n/a	n/a
5	BATF	chr7:53222928-53223116	GM12878	blood:	n/a	n/a
6	BATF	chr7:53224940-53225137	GM12878	blood:	n/a	n/a
7	BATF	chr7:53222915-53223110	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:53225473-53225789	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:53222919-53223087	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:53224929-53225120	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:53223246-53223532	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:53168041-53168066	HepG2	liver:	n/a	n/a
13	BHLHE40	chr7:53221742-53221948	HepG2	liver:	n/a	n/a
14	CBX3	chr7:53282259-53282412	K562	blood:	n/a	n/a
15	CEBPB	chr7:53231745-53231851	H1-hESC	embryonic stem cell:	n/a	chr7:53231795-53231808 chr7:53231797-53231806 chr7:53231795-53231808 chr7:53231796-53231807 chr7:53231795-53231806 chr7:53231795-53231808 chr7:53231797-53231806 chr7:53231797-53231806 chr7:53231797-53231806 chr7:53231795-53231806
16	CEBPB	chr7:53119101-53119192	K562	blood:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
17	CEBPB	chr7:53119013-53119280	A549	lung:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
18	CEBPB	chr7:53118958-53119292	IMR90	lung:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
19	CEBPB	chr7:53125684-53125704	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr7:53231661-53231887	IMR90	lung:	n/a	chr7:53231795-53231808 chr7:53231797-53231806 chr7:53231795-53231808 chr7:53231796-53231807 chr7:53231795-53231806 chr7:53231795-53231808 chr7:53231797-53231806 chr7:53231797-53231806 chr7:53231797-53231806 chr7:53231795-53231806
21	CEBPB	chr7:53118954-53119310	HepG2	liver:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
22	CEBPB	chr7:53207990-53208229	HepG2	liver:	n/a	chr7:53208124-53208135 chr7:53208110-53208123
23	CEBPB	chr7:53163859-53164112	HepG2	liver:	n/a	chr7:53163991-53164002 chr7:53163989-53164000
24	CEBPB	chr7:53252877-53253119	HepG2	liver:	n/a	chr7:53253037-53253048
25	CEBPB	chr7:53101896-53102047	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:53231685-53231960	HepG2	liver:	n/a	chr7:53231795-53231808 chr7:53231797-53231806 chr7:53231795-53231808 chr7:53231796-53231807 chr7:53231795-53231806 chr7:53231795-53231808 chr7:53231797-53231806 chr7:53231797-53231806 chr7:53231797-53231806 chr7:53231795-53231806
27	CEBPB	chr7:53252910-53253178	A549	lung:	n/a	chr7:53253037-53253048
28	CEBPB	chr7:53125637-53125841	HepG2	liver:	n/a	chr7:53125694-53125707
29	CEBPB	chr7:53346228-53346428	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:53117015-53117347	HepG2	liver:	n/a	chr7:53117164-53117177 chr7:53117164-53117177 chr7:53117164-53117177 chr7:53117164-53117175
31	CEBPB	chr7:53118946-53119288	H1-hESC	embryonic stem cell:	n/a	chr7:53119119-53119130 chr7:53119119-53119132 chr7:53119120-53119131 chr7:53119119-53119132 chr7:53119121-53119130
32	CHD1	chr7:53174071-53174383	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr7:53286698-53287309	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:53215680-53215830	NHEK	skin:	n/a	n/a
35	CTCF	chr7:53190685-53190714	GM10266	blood:	n/a	n/a
36	CTCF	chr7:53286800-53286950	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr7:53254969-53254989	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:53276952-53277086	Hela-S3	cervix:	n/a	chr7:53277013-53277022
39	CTCF	chr7:53210189-53210253	Medullo	brain:	n/a	n/a
40	CTCF	chr7:53276940-53277090	BE2_C	brain:	n/a	chr7:53277013-53277022
41	CTCF	chr7:53114918-53114945	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr7:53255063-53255089	A549	lung:	n/a	n/a
43	CTCF	chr7:53277001-53277043	GM10266	blood:	n/a	chr7:53277013-53277022
44	CTCF	chr7:53170302-53170346	Gliobla	brain:	n/a	n/a
45	CTCF	chr7:53276907-53277146	H1-hESC	embryonic stem cell:	n/a	chr7:53277013-53277022
46	CTCF	chr7:53276990-53277090	HUVEC	blood vessel:	n/a	chr7:53277013-53277022
47	CTCF	chr7:53339900-53340050	MCF-7	breast:	n/a	chr7:53339981-53339994
48	CTCF	chr7:53181720-53181733	GM13976	blood:	n/a	n/a
49	CTCF	chr7:53248307-53248360	GM13976	blood:	n/a	n/a
50	CTCF	chr7:53259195-53259197	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:53154966-53155016	SK-N-MC	brain:	n/a
2	chr7:53103285-53103335	AG10803	skin:	n/a
3	chr7:53305866-53305916	HIPEpiC	eye:	n/a
4	chr7:53154966-53155016	SK-N-MC	brain:	n/a
5	chr7:53103285-53103335	AG10803	skin:	n/a
6	chr7:53305866-53305916	HIPEpiC	eye:	n/a
7	chr7:53284941-53284991	HEK293	kidney:	embryo
8	chr7:53257327-53257377	Caco-2	colon:	n/a
9	chr7:53104001-53104051	U87	brain:	n/a
10	chr7:53255225-53255275	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:53182844-53182894	Hepatocyte	liver:	n/a
12	chr7:53103576-53103626	AG10803	skin:	n/a
13	chr7:53102721-53102771	HMEC	breast:	n/a
14	chr7:53254983-53255033	HepG2	liver:	n/a
15	chr7:53257327-53257377	NH-A	brain:	n/a
16	chr7:53287126-53287176	GM12892	blood:	n/a
17	chr7:53103214-53103264	BJ	skin:	n/a
18	chr7:53286906-53286956	NHBE	bronchial:	n/a
19	chr7:53286592-53286642	ProgFib	skin:	n/a
20	chr7:53103214-53103264	SK-N-SH_RA	brain:	n/a
21	chr7:53154966-53155016	MCF10A-Er-Src	breast:	n/a
22	chr7:53255225-53255275	SAEC	small airway:	n/a
23	chr7:53103789-53103839	NHDF-neo	bronchial:	n/a
24	chr7:53286592-53286642	HNPCEpiC	eye:	n/a
25	chr7:53102694-53102744	SAEC	small airway:	n/a
26	chr7:53287126-53287176	NHBE	bronchial:	n/a
27	chr7:53286906-53286956	HEEpiC	esophagus:	n/a
28	chr7:53102694-53102744	NH-A	brain:	n/a
29	chr7:53190606-53190656	NT2-D1	testis:	n/a
30	chr7:53102694-53102744	GM12891	blood:	n/a
31	chr7:53257327-53257377	AG10803	skin:	n/a
32	chr7:53103576-53103626	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:53286921-53286971	H1-hESC	embryonic stem cell:	embryo
34	chr7:53255203-53255253	NHDF-neo	bronchial:	n/a
35	chr7:53103789-53103839	GM12892	blood:	n/a
36	chr7:53155221-53155271	AG04449	skin:	fetal
37	chr7:53155221-53155271	BJ	skin:	n/a
38	chr7:53289011-53289061	ECC-1	luminal epithelium:	n/a
39	chr7:53155221-53155271	HNPCEpiC	eye:	n/a
40	chr7:53104001-53104051	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:53102694-53102744	SK-N-SH_RA	brain:	n/a
42	chr7:53103285-53103335	GM19239	blood:	n/a
43	chr7:53255225-53255275	MCF-7	breast:	n/a
44	chr7:53254947-53254997	PrEC	prostate:	n/a
45	chr7:53255203-53255253	HepG2	liver:	n/a
46	chr7:53254947-53254997	NT2-D1	testis:	n/a
47	chr7:53155107-53155157	HAEpiC	amniotic membrane:	n/a
48	chr7:53155107-53155157	AoSMC	blood vessel:	n/a
49	chr7:53283589-53283639	NH-A	brain:	n/a
50	chr7:53103214-53103264	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:53263027..53265803-chr7:53508163..53510506,2	K562	blood:
2	chr7:53213709..53216589-chr7:53219355..53221202,2	MCF-7	breast:
3	chr7:53155919..53158080-chr7:53165573..53167776,2	MCF-7	breast:
4	chr7:53154314..53155979-chr7:53166345..53169184,2	MCF-7	breast:
5	chr7:53157602..53160581-chr7:53161420..53163766,2	K562	blood:
6	chr22:19158805..19159401-chr7:53162782..53163559,2	MCF-7	breast:
7	chr7:53213709..53216589-chr7:53219355..53221202,2	MCF-7	breast:
8	chr4:71468407..71469255-chr7:53248075..53248575,2	HCT-116	colon:
9	chr7:53099169..53101604-chr7:53102398..53104340,2	MCF-7	breast:
10	chr7:53154314..53155979-chr7:53166345..53169184,2	MCF-7	breast:
11	chr7:53254389..53254893-chr9:19102491..19103022,3	NB4	blood:
12	chr7:53155919..53158080-chr7:53165573..53167776,2	MCF-7	breast:
13	chr7:53157602..53160581-chr7:53161420..53163766,2	K562	blood:
14	chr17:25277426..25278160-chr7:53200570..53201453,2	MCF-7	breast:
15	chr7:53104943..53106770-chr7:53108333..53110312,2	K562	blood:
16	chr7:53104943..53106770-chr7:53108333..53110312,2	K562	blood:
17	chr1:108671845..108673381-chr7:53151723..53153225,2	MCF-7	breast:

Variant related genes	Relation type
HAUS6P1	TF binding region
POM121L12	TF binding region
HAUS6P1	CpG island
POM121L12	CpG island
ENSG00000260924	chromatin interactions
ENSG00000221900	chromatin interactions

Extended variants
information (count: 3902 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:3902 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6964203	chr7:53099969-53099970	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140822414	chr7:53099971-53099972	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs11974343	chr7:53099987-53099988	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs561199915	chr7:53100004-53100005	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs62454552	chr7:53100017-53100018	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs112408347	chr7:53100020-53100021	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs549858517	chr7:53100046-53100047	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs6977554	chr7:53100051-53100052	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs6964356	chr7:53100058-53100059	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552035189	chr7:53100069-53100070	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564852424	chr7:53100071-53100072	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190577799	chr7:53100112-53100113	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534489665	chr7:53100130-53100131	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6977734	chr7:53100146-53100147	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568022735	chr7:53100147-53100148	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs56345578	chr7:53100194-53100195	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73698758	chr7:53100209-53100210	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs576899457	chr7:53100211-53100212	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs180825759	chr7:53100219-53100220	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs953842	chr7:53100235-53100236	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116468471	chr7:53100265-53100266	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs6960678	chr7:53100268-53100269	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs541234143	chr7:53100275-53100276	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561434801	chr7:53100279-53100280	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2330339	chr7:53100319-53100320	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs543887344	chr7:53100325-53100326	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563373010	chr7:53100332-53100333	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141679043	chr7:53100346-53100347	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577395327	chr7:53100385-53100386	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs150770431	chr7:53100407-53100408	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565602942	chr7:53100422-53100423	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554662452	chr7:53100518-53100519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs62454553	chr7:53100519-53100520	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116162152	chr7:53100529-53100530	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184456637	chr7:53100584-53100585	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370547811	chr7:53100675-53100676	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575980074	chr7:53100697-53100698	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79550985	chr7:53100699-53100700	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557077382	chr7:53100700-53100701	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138048336	chr7:53100719-53100720	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189731700	chr7:53100732-53100733	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371506955	chr7:53100735-53100736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559310465	chr7:53100736-53100737	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149533028	chr7:53100754-53100755	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs541706394	chr7:53100765-53100766	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554902701	chr7:53100770-53100771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574958315	chr7:53100809-53100810	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12718736	chr7:53100822-53100823	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181248353	chr7:53100824-53100825	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532386622	chr7:53100905-53100906	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53099600-53100000	Active TSS	H9 Cell Line	embryonic stem cell
2	chr7:53099600-53100000	Active TSS	Placenta	Placenta
3	chr7:53099600-53100200	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr7:53099600-53100200	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr7:53099600-53100200	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr7:53099800-53100400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr7:53103400-53103800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:53103400-53104000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:53104000-53104200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:53104200-53104400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:53108000-53108200	Enhancers	Ovary	ovary
12	chr7:53108400-53109600	Weak transcription	Ovary	ovary
13	chr7:53109600-53110000	Enhancers	Ovary	ovary
14	chr7:53110000-53111600	Weak transcription	Ovary	ovary
15	chr7:53111600-53111800	Enhancers	Aorta	Aorta
16	chr7:53111600-53111800	Enhancers	Ovary	ovary
17	chr7:53111800-53112200	Weak transcription	Aorta	Aorta
18	chr7:53115000-53115200	Enhancers	Brain Substantia Nigra	brain
19	chr7:53115600-53117200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:53115600-53118000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:53117200-53118400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr7:53118200-53118400	Enhancers	Brain Substantia Nigra	brain
23	chr7:53118400-53119800	Weak transcription	Brain Substantia Nigra	brain
24	chr7:53127200-53127400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:53127200-53127600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr7:53127600-53129000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:53129400-53131000	Enhancers	Brain Hippocampus Middle	brain
28	chr7:53130000-53130600	Enhancers	Brain Cingulate Gyrus	brain
29	chr7:53130400-53131200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr7:53138400-53139800	Enhancers	HUVEC	blood vessel
31	chr7:53138600-53139400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:53138600-53143800	Weak transcription	Aorta	Aorta
33	chr7:53143800-53144200	ZNF genes & repeats	Aorta	Aorta
34	chr7:53146600-53147000	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr7:53146800-53147000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr7:53154800-53155400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:53162000-53162800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr7:53162400-53164800	Enhancers	HUVEC	blood vessel
39	chr7:53162600-53162800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:53164000-53164400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:53164800-53167200	Weak transcription	HUVEC	blood vessel
42	chr7:53165400-53166000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:53166000-53167000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:53167000-53167400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr7:53167200-53168600	Enhancers	HUVEC	blood vessel
46	chr7:53178000-53179200	Enhancers	Fetal Muscle Leg	muscle
47	chr7:53178000-53180000	Enhancers	Fetal Heart	heart
48	chr7:53178200-53178400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr7:53178200-53179000	Enhancers	NH-A	brain
50	chr7:53178400-53185800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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