Variant report

Variant	nsv607010
Chromosome Location	chr7:53262051-53570145
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:731)
CpG islands
(count:610)
Chromatin interactive
region (count:15)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:53486223-53486324	K562	blood:	n/a	n/a
2	BACH1	chr7:53286655-53287303	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr7:53394310-53394736	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr7:53282259-53282412	K562	blood:	n/a	n/a
5	CEBPB	chr7:53408869-53409149	IMR90	lung:	n/a	chr7:53409007-53409018
6	CEBPB	chr7:53530560-53530856	H1-hESC	embryonic stem cell:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
7	CEBPB	chr7:53501358-53501394	H1-hESC	embryonic stem cell:	n/a	chr7:53501375-53501386
8	CEBPB	chr7:53502040-53502264	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:53505078-53505387	HepG2	liver:	n/a	chr7:53505251-53505262
10	CEBPB	chr7:53501208-53501545	HepG2	liver:	n/a	chr7:53501375-53501386
11	CEBPB	chr7:53346228-53346428	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:53505120-53505352	Hela-S3	cervix:	n/a	chr7:53505251-53505262
13	CEBPB	chr7:53432286-53432571	HepG2	liver:	n/a	chr7:53432454-53432465 chr7:53432423-53432434
14	CEBPB	chr7:53530548-53530869	IMR90	lung:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
15	CEBPB	chr7:53530516-53530859	K562	blood:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
16	CEBPB	chr7:53501299-53501500	IMR90	lung:	n/a	chr7:53501375-53501386
17	CEBPB	chr7:53501280-53501444	K562	blood:	n/a	chr7:53501375-53501386
18	CEBPB	chr7:53437537-53437772	HepG2	liver:	n/a	chr7:53437678-53437691 chr7:53437679-53437690
19	CEBPB	chr7:53432896-53433292	MCF-7	breast:	n/a	n/a
20	CEBPB	chr7:53370596-53370856	H1-hESC	embryonic stem cell:	n/a	chr7:53370730-53370741 chr7:53370730-53370743
21	CEBPB	chr7:53408853-53409171	HepG2	liver:	n/a	chr7:53409007-53409018
22	CEBPB	chr7:53530536-53530863	HepG2	liver:	n/a	chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530708 chr7:53530697-53530706 chr7:53530695-53530706 chr7:53530697-53530706
23	CEBPB	chr7:53377863-53378110	HepG2	liver:	n/a	chr7:53377942-53377953
24	CEBPB	chr7:53392769-53393306	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr7:53383676-53384015	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr7:53392818-53393166	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr7:53394245-53394766	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTBP2	chr7:53286698-53287309	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:53488240-53488244	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr7:53418080-53418230	GM12878	blood:	n/a	n/a
31	CTCF	chr7:53417908-53418281	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:53418040-53418190	GM12866	blood:	n/a	n/a
33	CTCF	chr7:53276990-53277090	HUVEC	blood vessel:	n/a	chr7:53277013-53277022
34	CTCF	chr7:53426132-53426288	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:53418002-53418247	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr7:53516240-53516390	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr7:53418084-53418172	GM19239	blood:	n/a	n/a
38	CTCF	chr7:53567900-53568050	HMEC	breast:	n/a	n/a
39	CTCF	chr7:53418069-53418200	Lung_OC	lung:	n/a	n/a
40	CTCF	chr7:53418060-53418210	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr7:53276932-53277109	MCF-7	breast:	n/a	chr7:53277013-53277022
42	CTCF	chr7:53426139-53426247	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr7:53418040-53418190	NB4	blood:	n/a	n/a
44	CTCF	chr7:53426144-53426186	LNCaP	prostate:	n/a	n/a
45	CTCF	chr7:53411599-53411617	GM20000	blood:	n/a	n/a
46	CTCF	chr7:53324160-53324310	WI-38	lung:	n/a	n/a
47	CTCF	chr7:53285398-53285540	K562	blood:	n/a	n/a
48	CTCF	chr7:53426140-53426290	A549	lung:	n/a	n/a
49	CTCF	chr7:53494240-53494390	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr7:53488120-53488270	RPTEC	kidney:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:53286921-53286971	Hepatocyte	liver:	n/a
2	chr7:53290696-53290746	GM12892	blood:	n/a
3	chr7:53290696-53290746	NHDF-neo	bronchial:	n/a
4	chr7:53290696-53290746	Caco-2	colon:	n/a
5	chr7:53284941-53284991	SK-N-MC	brain:	n/a
6	chr7:53393696-53393746	CMK	blood:	n/a
7	chr7:53393696-53393746	HNPCEpiC	eye:	n/a
8	chr7:53286906-53286956	BJ	skin:	n/a
9	chr7:53289011-53289061	IMR90	lung:	fetal
10	chr7:53305866-53305916	HRCEpiC	kidney:	n/a
11	chr7:53305866-53305916	HAEpiC	amniotic membrane:	n/a
12	chr7:53287126-53287176	HRPEpiC	eye:	n/a
13	chr7:53284941-53284991	K562	blood:	n/a
14	chr7:53283589-53283639	HNPCEpiC	eye:	n/a
15	chr7:53286906-53286956	HepG2	liver:	n/a
16	chr7:53283589-53283639	AG09319	gingival:	n/a
17	chr7:53286592-53286642	HRCEpiC	kidney:	n/a
18	chr7:53287126-53287176	HAEpiC	amniotic membrane:	n/a
19	chr7:53287126-53287176	SK-N-SH_RA	brain:	n/a
20	chr7:53286592-53286642	NHBE	bronchial:	n/a
21	chr7:53290696-53290746	Hepatocyte	liver:	n/a
22	chr7:53393696-53393746	RPTEC	kidney:	n/a
23	chr7:53284941-53284991	NHBE	bronchial:	n/a
24	chr7:53289011-53289061	U87	brain:	n/a
25	chr7:53287126-53287176	Hepatocyte	liver:	n/a
26	chr7:53393696-53393746	BE2_C	brain:	n/a
27	chr7:53286921-53286971	GM19239	blood:	n/a
28	chr7:53305866-53305916	HEK293	kidney:	embryo
29	chr7:53283589-53283639	PFSK-1	brain:	n/a
30	chr7:53283589-53283639	GM12892	blood:	n/a
31	chr7:53290696-53290746	PFSK-1	brain:	n/a
32	chr7:53286906-53286956	Jurkat	blood:	n/a
33	chr7:53290696-53290746	IMR90	lung:	fetal
34	chr7:53305866-53305916	SKMC	muscle:	n/a
35	chr7:53286921-53286971	SK-N-SH_RA	brain:	n/a
36	chr7:53286921-53286971	PrEC	prostate:	n/a
37	chr7:53290696-53290746	T-47D	breast:	n/a
38	chr7:53393696-53393746	HEK293	kidney:	embryo
39	chr7:53287126-53287176	H1-hESC	embryonic stem cell:	embryo
40	chr7:53283589-53283639	CMK	blood:	n/a
41	chr7:53305866-53305916	A549	lung:	n/a
42	chr7:53286921-53286971	HRCEpiC	kidney:	n/a
43	chr7:53286906-53286956	H1-hESC	embryonic stem cell:	embryo
44	chr7:53286921-53286971	Hela-S3	cervix:	n/a
45	chr7:53286906-53286956	HNPCEpiC	eye:	n/a
46	chr7:53286592-53286642	Hela-S3	cervix:	n/a
47	chr7:53286921-53286971	NB4	blood:	n/a
48	chr7:53283589-53283639	GM19239	blood:	n/a
49	chr7:53283589-53283639	BJ	skin:	n/a
50	chr7:53286906-53286956	MCF-7	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:53440139..53442287-chr7:53444229..53445943,2	MCF-7	breast:
2	chr7:53460851..53461831-chr9:14244620..14245120,2	MCF-7	breast:
3	chr7:53480788..53483198-chr7:53496726..53498453,2	K562	blood:
4	chr7:53480788..53483198-chr7:53496726..53498453,2	K562	blood:
5	chr7:53372759..53375444-chr7:53379362..53381261,2	K562	blood:
6	chr7:53372759..53375444-chr7:53379362..53381261,2	K562	blood:
7	chr7:53417753..53418714-chr7:54732235..54733019,3	MCF-7	breast:
8	chr7:53499272..53501434-chr7:53507043..53509851,2	K562	blood:
9	chr20:52720034..52720613-chr7:53479832..53480332,2	MCF-7	breast:
10	chr7:53263027..53265803-chr7:53508163..53510506,2	K562	blood:
11	chr7:53473728..53475869-chr7:53482133..53483752,2	K562	blood:
12	chr7:53473728..53475869-chr7:53482133..53483752,2	K562	blood:
13	chr7:53440139..53442287-chr7:53444229..53445943,2	MCF-7	breast:
14	chr7:53263027..53265803-chr7:53508163..53510506,2	K562	blood:
15	chr7:53499272..53501434-chr7:53507043..53509851,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEC61G-7	chr7:53486490-53486571	XLOC_006444
2	lnc-SEC61G-7	chr7:53466103-53466276	NONHSAT120628
3	lnc-SEC61G-7	chr7:53448220-53448434	NONHSAT120631
4	lnc-SEC61G-7	chr7:53448220-53448434	NONHSAT120626
5	lnc-SEC61G-7	chr7:53433793-53433894	NONHSAT120630
6	lnc-SEC61G-7	chr7:53486490-53486578	NONHSAT120631
7	lnc-SEC61G-7	chr7:53428227-53428251	NONHSAT120628
8	lnc-SEC61G-7	chr7:53448225-53448434	NONHSAT120635
9	lnc-SEC61G-7	chr7:53428227-53428251	NONHSAT120626
10	lnc-SEC61G-7	chr7:53466103-53466198	XLOC_006444
11	lnc-SEC61G-7	chr7:53448226-53448434	XLOC_006444
12	lnc-SEC61G-7	chr7:53448220-53448434	NONHSAT120628
13	lnc-SEC61G-7	chr7:53466102-53466198	NONHSAT120635
14	lnc-SEC61G-7	chr7:53428227-53428251	NONHSAT120627
15	lnc-SEC61G-7	chr7:53484018-53484072	NONHSAT120633
16	lnc-SEC61G-7	chr7:53448220-53448434	NONHSAT120627
17	lnc-SEC61G-7	chr7:53448122-53448434	NONHSAT120634
18	lnc-SEC61G-7	chr7:53484018-53484120	NONHSAT120626
19	lnc-SEC61G-7	chr7:53486490-53486585	NONHSAT120632
20	lnc-SEC61G-7	chr7:53486490-53486506	NONHSAT120627
21	lnc-SEC61G-7	chr7:53448122-53448434	NONHSAT120633
22	lnc-SEC61G-7	chr7:53466103-53466196	NONHSAT120634
23	lnc-POM121L12-6	chr7:53383842-53384433	NONHSAT120625
24	lnc-SEC61G-7	chr7:53448122-53448434	NONHSAT120632
25	lnc-SEC61G-12	chr7:53557841-53558132	NONHSAT120636
26	lnc-SEC61G-7	chr7:53448220-53448434	NONHSAT120630
27	lnc-SEC61G-7	chr7:53466103-53466322	NONHSAT120630
28	lnc-SEC61G-7	chr7:53433793-53433894	NONHSAT120631
29	lnc-SEC61G-7	chr7:53448226-53448434	XLOC_006444

No data

Variant related genes	Relation type
RN7SKP218	TF binding region
RNU1-14P	TF binding region
ENSG00000271194	TF binding region
RN7SKP218	CpG island
RNU1-14P	CpG island
ENSG00000271194	CpG island
CNOT6	miRNA target sites
MEIS1	miRNA target sites

Extended variants
information (count: 6452 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:6452 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371089182	chr7:53269807-53269808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376099381	chr7:53269838-53269839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10251336	chr7:53269864-53269865	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs540195378	chr7:53269875-53269876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553402446	chr7:53269886-53269887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370736093	chr7:53269896-53269897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542058977	chr7:53269899-53269900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561943772	chr7:53269900-53269901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs66462233	chr7:53269928-53269929	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs544071432	chr7:53269941-53269942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562653526	chr7:53269943-53269944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150847939	chr7:53269960-53269961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs386713343	chr7:53269971-53269972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10264763	chr7:53269973-53269974	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs73116740	chr7:53269990-53269991	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs529141895	chr7:53270003-53270004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532989159	chr7:53270022-53270023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73116744	chr7:53270025-53270026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73116745	chr7:53270035-53270036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs374875198	chr7:53270072-53270073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571283321	chr7:53270109-53270110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116097812	chr7:53270118-53270119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553680121	chr7:53270133-53270134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12670493	chr7:53270143-53270144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs66905734	chr7:53270241-53270242	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145127726	chr7:53270244-53270245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111695181	chr7:53270256-53270257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555577855	chr7:53270262-53270263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562008985	chr7:53270284-53270285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140079054	chr7:53270285-53270286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199621473	chr7:53270286-53270287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551230154	chr7:53270288-53270289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372839071	chr7:53270299-53270300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529039604	chr7:53270307-53270308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73370054	chr7:53270310-53270311	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190409772	chr7:53270318-53270319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564256347	chr7:53270372-53270373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533425190	chr7:53270384-53270385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181858869	chr7:53270457-53270458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560536491	chr7:53270483-53270484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529206846	chr7:53270497-53270498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549276853	chr7:53270510-53270511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75648581	chr7:53270512-53270513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75408791	chr7:53270516-53270517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571662432	chr7:53270530-53270531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80208703	chr7:53270536-53270537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571255591	chr7:53270546-53270547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs67414631	chr7:53270568-53270569	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs138223921	chr7:53270578-53270579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1525560	chr7:53270584-53270585	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:125)

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
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
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53269800-53270200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr7:53269800-53270600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:53277000-53277200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr7:53278800-53279200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:53279000-53279400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr7:53279000-53279600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr7:53279000-53279800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr7:53279000-53279800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr7:53279000-53280000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr7:53279200-53279800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:53279600-53280200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr7:53280800-53281600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr7:53282800-53283800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:53283400-53283800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr7:53285800-53286200	Enhancers	HUVEC	blood vessel
16	chr7:53286000-53286400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
17	chr7:53286000-53286400	Enhancers	Brain Germinal Matrix	brain
18	chr7:53286000-53286400	Enhancers	Brain Hippocampus Middle	brain
19	chr7:53286200-53286400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
20	chr7:53286200-53286400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:53286200-53286400	Flanking Active TSS	HUVEC	blood vessel
22	chr7:53286200-53286800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
23	chr7:53286400-53286600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr7:53286400-53286600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
25	chr7:53286400-53286600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr7:53286400-53286600	Flanking Active TSS	Brain Germinal Matrix	brain
27	chr7:53286400-53286600	Active TSS	Brain Hippocampus Middle	brain
28	chr7:53286400-53286600	Active TSS	Fetal Brain Female	brain
29	chr7:53286400-53286600	Active TSS	Fetal Muscle Leg	muscle
30	chr7:53286400-53286800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
31	chr7:53286400-53286800	Active TSS	Fetal Muscle Trunk	muscle
32	chr7:53286400-53286800	Active TSS	Fetal Stomach	stomach
33	chr7:53286400-53286800	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr7:53286400-53287200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:53286400-53287200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:53286400-53287200	Active TSS	Brain Anterior Caudate	brain
37	chr7:53286400-53287200	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr7:53286400-53287200	Active TSS	Brain Substantia Nigra	brain
39	chr7:53286400-53287200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
40	chr7:53286400-53287200	Active TSS	NH-A	brain
41	chr7:53286400-53287400	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr7:53286400-53287400	Active TSS	H9 Cell Line	embryonic stem cell
43	chr7:53286400-53287400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
44	chr7:53286400-53287400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr7:53286400-53287400	Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr7:53286400-53287400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:53286400-53287400	Active TSS	Aorta	Aorta
48	chr7:53286400-53287400	Active TSS	Brain Cingulate Gyrus	brain
49	chr7:53286400-53287400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr7:53286400-53287400	Active TSS	Colon Smooth Muscle	Colon

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