Variant report

Variant	nsv829686
Chromosome Location	chr3:116325622-116494541
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	ARID3A	chr3:116489695-116490043	HepG2	liver:	n/a	n/a
2	BHLHE40	chr3:116329061-116329146	HepG2	liver:	n/a	n/a
3	BRCA1	chr3:116414509-116414701	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr3:116489726-116490053	K562	blood:	n/a	n/a
5	CBX3	chr3:116489758-116489965	K562	blood:	n/a	n/a
6	CEBPB	chr3:116376019-116376253	HepG2	liver:	n/a	n/a
7	CEBPB	chr3:116380085-116380437	IMR90	lung:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
8	CEBPB	chr3:116438399-116438554	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:116409929-116410256	IMR90	lung:	n/a	chr3:116410093-116410104
10	CEBPB	chr3:116371261-116371583	A549	lung:	n/a	chr3:116371433-116371444
11	CEBPB	chr3:116380104-116380421	HepG2	liver:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
12	CEBPB	chr3:116460375-116460682	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr3:116413104-116413373	A549	lung:	n/a	n/a
14	CEBPB	chr3:116380163-116380363	H1-hESC	embryonic stem cell:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
15	CEBPB	chr3:116376019-116376294	IMR90	lung:	n/a	n/a
16	CEBPB	chr3:116444331-116444582	HepG2	liver:	n/a	chr3:116444424-116444435 chr3:116444426-116444435
17	CEBPB	chr3:116468969-116469052	A549	lung:	n/a	n/a
18	CEBPB	chr3:116371274-116371609	IMR90	lung:	n/a	chr3:116371433-116371444
19	CEBPB	chr3:116409913-116410250	A549	lung:	n/a	chr3:116410093-116410104
20	CEBPB	chr3:116447456-116447605	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:116371294-116371606	H1-hESC	embryonic stem cell:	n/a	chr3:116371433-116371444
22	CEBPB	chr3:116447484-116447512	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:116421243-116421563	HepG2	liver:	n/a	chr3:116421416-116421427 chr3:116421414-116421431 chr3:116421415-116421426 chr3:116421415-116421428 chr3:116421415-116421428
24	CEBPB	chr3:116409918-116410249	HepG2	liver:	n/a	chr3:116410093-116410104
25	CEBPB	chr3:116376093-116376293	A549	lung:	n/a	n/a
26	CEBPB	chr3:116471779-116471796	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:116447561-116447595	A549	lung:	n/a	n/a
28	CEBPB	chr3:116447345-116447641	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr3:116409978-116410160	H1-hESC	embryonic stem cell:	n/a	chr3:116410093-116410104
30	CEBPB	chr3:116421337-116421535	A549	lung:	n/a	chr3:116421416-116421427 chr3:116421414-116421431 chr3:116421415-116421426 chr3:116421415-116421428 chr3:116421415-116421428
31	CEBPB	chr3:116380110-116380418	A549	lung:	n/a	chr3:116380267-116380276 chr3:116380267-116380276 chr3:116380265-116380276 chr3:116380267-116380276 chr3:116380267-116380278 chr3:116380267-116380276
32	CEBPB	chr3:116434246-116434422	A549	lung:	n/a	n/a
33	CEBPB	chr3:116460425-116460556	HepG2	liver:	n/a	n/a
34	CEBPB	chr3:116489628-116490015	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:116371270-116371597	HepG2	liver:	n/a	chr3:116371433-116371444
36	CHD1	chr3:116490173-116490300	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr3:116489699-116490053	GM13977	blood:	n/a	chr3:116489914-116489932 chr3:116489834-116489855 chr3:116489915-116489931 chr3:116489832-116489850
38	CTCF	chr3:116477190-116477275	H1-hESC	embryonic stem cell:	n/a	chr3:116477235-116477248 chr3:116477199-116477207 chr3:116477233-116477251 chr3:116477234-116477250
39	CTCF	chr3:116477200-116477350	GM12865	blood:	n/a	chr3:116477235-116477248 chr3:116477233-116477251 chr3:116477234-116477250
40	CTCF	chr3:116489800-116489950	AG04450	lung:	n/a	chr3:116489914-116489932 chr3:116489834-116489855 chr3:116489915-116489931 chr3:116489832-116489850
41	CTCF	chr3:116477115-116477385	GM12878	blood:	n/a	chr3:116477235-116477248 chr3:116477199-116477207 chr3:116477233-116477251 chr3:116477234-116477250
42	CTCF	chr3:116477137-116477370	GM10248	blood:	n/a	chr3:116477235-116477248 chr3:116477199-116477207 chr3:116477233-116477251 chr3:116477234-116477250
43	CTCF	chr3:116333780-116333930	HEK293	kidney:	n/a	chr3:116333827-116333848 chr3:116333828-116333837 chr3:116333825-116333843
44	CTCF	chr3:116333725-116333947	Hela-S3	cervix:	n/a	chr3:116333827-116333848 chr3:116333828-116333837 chr3:116333825-116333843
45	CTCF	chr3:116477123-116477382	Pancreas_OC	pancreas:	n/a	chr3:116477235-116477248 chr3:116477199-116477207 chr3:116477233-116477251 chr3:116477234-116477250
46	CTCF	chr3:116489780-116489930	A549	lung:	n/a	chr3:116489834-116489855 chr3:116489832-116489850
47	CTCF	chr3:116489760-116489910	BE2_C	brain:	n/a	chr3:116489834-116489855 chr3:116489832-116489850
48	CTCF	chr3:116489721-116490019	GM20000	blood:	n/a	chr3:116489914-116489932 chr3:116489834-116489855 chr3:116489915-116489931 chr3:116489832-116489850
49	CTCF	chr3:116489707-116490030	Hela-S3	cervix:	n/a	chr3:116489914-116489932 chr3:116489834-116489855 chr3:116489915-116489931 chr3:116489832-116489850
50	CTCF	chr3:116477140-116477290	K562	blood:	n/a	chr3:116477235-116477248 chr3:116477199-116477207 chr3:116477233-116477251 chr3:116477234-116477250

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:116432221-116432271	HepG2	liver:	n/a
2	chr3:116428385-116428435	RPTEC	kidney:	n/a
3	chr3:116476085-116476135	HIPEpiC	eye:	n/a
4	chr3:116476085-116476135	HMEC	breast:	n/a
5	chr3:116476085-116476135	ECC-1	luminal epithelium:	n/a
6	chr3:116432221-116432271	HPAEpiC	pulmonary alveolar:	n/a
7	chr3:116432221-116432271	GM12892	blood:	n/a
8	chr3:116428610-116428660	NHBE	bronchial:	n/a
9	chr3:116428101-116428151	ProgFib	skin:	n/a
10	chr3:116437373-116437423	ovcar-3	ovarian:	n/a
11	chr3:116428101-116428151	GM12892	blood:	n/a
12	chr3:116476085-116476135	ovcar-3	ovarian:	n/a
13	chr3:116437373-116437423	HRPEpiC	eye:	n/a
14	chr3:116432221-116432271	A549	lung:	n/a
15	chr3:116428610-116428660	NB4	blood:	n/a
16	chr3:116432221-116432271	ovcar-3	ovarian:	n/a
17	chr3:116366327-116366377	H1-hESC	embryonic stem cell:	embryo
18	chr3:116428385-116428435	AG10803	skin:	n/a
19	chr3:116428101-116428151	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:116428385-116428435	GM12891	blood:	n/a
21	chr3:116366327-116366377	HepG2	liver:	n/a
22	chr3:116432221-116432271	AG09309	skin:	n/a
23	chr3:116432221-116432271	Jurkat	blood:	n/a
24	chr3:116437373-116437423	NHDF-neo	bronchial:	n/a
25	chr3:116428101-116428151	CMK	blood:	n/a
26	chr3:116428385-116428435	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:116428610-116428660	HRPEpiC	eye:	n/a
28	chr3:116437373-116437423	HEEpiC	esophagus:	n/a
29	chr3:116437373-116437423	HRCEpiC	kidney:	n/a
30	chr3:116476085-116476135	LNCaP	prostate:	n/a
31	chr3:116437373-116437423	AG10803	skin:	n/a
32	chr3:116428101-116428151	HEK293	kidney:	embryo
33	chr3:116432221-116432271	HIPEpiC	eye:	n/a
34	chr3:116437373-116437423	PrEC	prostate:	n/a
35	chr3:116476085-116476135	AG09309	skin:	n/a
36	chr3:116428101-116428151	HAEpiC	amniotic membrane:	n/a
37	chr3:116366327-116366377	AoSMC	blood vessel:	n/a
38	chr3:116428610-116428660	HIPEpiC	eye:	n/a
39	chr3:116476085-116476135	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:116428385-116428435	SAEC	small airway:	n/a
41	chr3:116437373-116437423	HCF	heart:	n/a
42	chr3:116437373-116437423	HepG2	liver:	n/a
43	chr3:116428101-116428151	SK-N-SH	brain:	n/a
44	chr3:116476085-116476135	HRCEpiC	kidney:	n/a
45	chr3:116437373-116437423	HNPCEpiC	eye:	n/a
46	chr3:116432221-116432271	HL-60	blood:	n/a
47	chr3:116428101-116428151	HIPEpiC	eye:	n/a
48	chr3:116476085-116476135	MCF10A-Er-Src	breast:	n/a
49	chr3:116432221-116432271	GM12891	blood:	n/a
50	chr3:116437373-116437423	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:116333627..116334309-chr3:116476779..116477665,2	MCF-7	breast:
2	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
3	chr3:116489744..116490282-chr3:117438266..117438796,2	MCF-7	breast:
4	chr3:116489375..116490293-chr3:117716457..117716989,3	K562	blood:
5	chr3:116489418..116490481-chr3:116582039..116583181,3	MCF-7	breast:
6	chr3:116333340..116334182-chr3:116476544..116477667,3	MCF-7	breast:
7	chr3:116317000..116318575-chr3:116380678..116383155,2	K562	blood:
8	chr3:116333340..116334182-chr3:116476544..116477667,3	MCF-7	breast:
9	chr3:116333627..116334309-chr3:116476779..116477665,2	MCF-7	breast:
10	chr3:116489400..116490326-chr3:117437986..117438758,2	K562	blood:
11	chr3:116489426..116490301-chr3:117268289..117269096,2	MCF-7	breast:
12	chr3:116446011..116448567-chr3:116450501..116453384,2	K562	blood:
13	chr3:116446011..116448567-chr3:116450501..116453384,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GAP43-6	chr3:116431202-116431704	NONHSAT091317
2	lnc-GAP43-6	chr3:116428680-116428723	ENSG00000243197.1
3	lnc-GAP43-6	chr3:116442199-116442428	ENSG00000243197.1
4	lnc-GAP43-6	chr3:116436608-116436765	ENSG00000243197.1
5	lnc-GAP43-6	chr3:116435035-116435278	ENSG00000243197.1
6	lnc-GAP43-6	chr3:116431202-116431354	ENSG00000243197.1
7	lnc-GAP43-6	chr3:116435035-116436168	ENSG00000243197.3
8	lnc-GAP43-6	chr3:116429051-116429268	ENSG00000243197.1
9	lnc-GAP43-6	chr3:116432886-116432997	NONHSAT091317
10	lnc-GAP43-6	chr3:116429051-116429268	ENSG00000243197.3
11	lnc-GAP43-6	chr3:116428816-116429268	ENSG00000243197.1
12	lnc-GAP43-6	chr3:116428253-116429268	ENSG00000243197.3
13	lnc-GAP43-6	chr3:116428082-116428907	ENSG00000243197.3
14	lnc-GAP43-6	chr3:116431202-116431354	ENSG00000243197.3
15	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.3
16	lnc-GAP43-6	chr3:116431202-116431354	ENSG00000243197.1
17	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
18	lnc-GAP43-6	chr3:116435035-116435278	ENSG00000243197.1
19	lnc-GAP43-6	chr3:116431202-116431318	ENSG00000243197.1
20	lnc-GAP43-6	chr3:116435035-116435817	NONHSAT091316
21	lnc-GAP43-6	chr3:116428816-116429268	ENSG00000243197.1
22	lnc-GAP43-6	chr3:116435035-116435282	ENSG00000243197.1
23	lnc-GAP43-6	chr3:116431202-116431354	NONHSAT091316
24	lnc-GAP43-6	chr3:116435035-116435817	NONHSAT091317
25	lnc-GAP43-6	chr3:116431202-116431318	ENSG00000243197.3
26	lnc-GAP43-6	chr3:116428626-116429268	ENSG00000243197.1
27	lnc-GAP43-6	chr3:116429051-116429268	NONHSAT091316
28	lnc-GAP43-6	chr3:116428671-116428907	ENSG00000243197.1
29	lnc-GAP43-6	chr3:116432886-116432997	NONHSAT091315
30	lnc-GAP43-6	chr3:116431202-116431446	ENSG00000243197.1
31	lnc-GAP43-6	chr3:116428636-116428907	NONHSAT091316
32	lnc-GAP43-6	chr3:116428635-116429268	NONHSAT091315
33	lnc-GAP43-6	chr3:116428636-116428723	NONHSAT091317
34	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.3
35	lnc-GAP43-6	chr3:116428626-116428723	ENSG00000243197.1
36	lnc-GAP43-6	chr3:116431202-116431704	ENSG00000243197.1
37	lnc-GAP43-6	chr3:116432886-116432997	NONHSAT091316
38	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
39	lnc-GAP43-6	chr3:116435035-116435878	ENSG00000243197.1
40	lnc-GAP43-6	chr3:116431202-116431704	NONHSAT091315
41	lnc-GAP43-6	chr3:116435035-116435174	ENSG00000243197.3
42	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
43	lnc-GAP43-6	chr3:116432886-116432997	ENSG00000243197.1
44	lnc-GAP43-6	chr3:116435035-116435887	NONHSAT091315
45	lnc-GAP43-6	chr3:116428606-116428723	ENSG00000243197.3
46	lnc-GAP43-6	chr3:116431202-116431704	ENSG00000243197.3

Variant related genes	Relation type
BZW1P2	TF binding region
TUSC7	TF binding region
BZW1P2	CpG island
TUSC7	CpG island

Extended variants
information (count: 3450 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3450 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546977103	chr3:116325630-116325631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115445229	chr3:116325672-116325673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370499743	chr3:116325673-116325674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538807974	chr3:116325678-116325679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111654635	chr3:116325694-116325695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4370025	chr3:116325700-116325701	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114658709	chr3:116325709-116325710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4389475	chr3:116325718-116325719	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs561112186	chr3:116325720-116325721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573921292	chr3:116325743-116325744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386664902	chr3:116325748-116325749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200365196	chr3:116325749-116325750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11929011	chr3:116325750-116325751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140413751	chr3:116325763-116325764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11929035	chr3:116325786-116325787	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192138121	chr3:116325789-116325790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554182746	chr3:116325803-116325804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371937401	chr3:116325807-116325808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548996030	chr3:116325832-116325833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567148802	chr3:116325840-116325841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11914365	chr3:116325872-116325873	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546987978	chr3:116325873-116325874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571876326	chr3:116325882-116325883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549143977	chr3:116325993-116325994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58065625	chr3:116325999-116326000	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs557113770	chr3:116326022-116326023	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs34305283	chr3:116326082-116326083	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs536340284	chr3:116326106-116326107	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs150345283	chr3:116326128-116326129	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs557552647	chr3:116326158-116326159	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs9809762	chr3:116326159-116326160	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540163064	chr3:116326162-116326163	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs375215403	chr3:116326198-116326199	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577978543	chr3:116326231-116326232	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183863786	chr3:116326280-116326281	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs62271987	chr3:116326284-116326285	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs11914482	chr3:116326293-116326294	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs575433531	chr3:116326356-116326357	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375903591	chr3:116326408-116326409	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs530662376	chr3:116326427-116326428	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544375638	chr3:116326436-116326437	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs548808426	chr3:116326438-116326439	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376842434	chr3:116326439-116326440	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138054074	chr3:116326451-116326452	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs11926418	chr3:116326459-116326460	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs111923413	chr3:116326460-116326461	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs571638669	chr3:116326471-116326472	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373094327	chr3:116326483-116326484	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533204541	chr3:116326485-116326486	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs188535573	chr3:116326487-116326488	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116325600-116326400	Enhancers	Brain Substantia Nigra	brain
2	chr3:116325600-116326800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:116325800-116326000	Enhancers	Brain Hippocampus Middle	brain
4	chr3:116325800-116326400	Enhancers	Brain Cingulate Gyrus	brain
5	chr3:116326000-116326600	Flanking Active TSS	Brain Hippocampus Middle	brain
6	chr3:116326000-116326600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr3:116326000-116326600	Active TSS	Spleen	Spleen
8	chr3:116326200-116326600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:116326600-116326800	Enhancers	Brain Hippocampus Middle	brain
10	chr3:116328200-116328400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:116328400-116329800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:116329800-116330000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:116337000-116337400	Enhancers	HMEC	breast
14	chr3:116337000-116337600	Enhancers	NHEK	skin
15	chr3:116337000-116337800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr3:116337000-116338000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr3:116338000-116340600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr3:116340600-116341000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr3:116340600-116341000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:116340600-116341200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:116352200-116352400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:116352400-116353400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:116353200-116353600	Enhancers	Brain Substantia Nigra	brain
24	chr3:116353400-116354000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:116353400-116354000	Active TSS	Brain Hippocampus Middle	brain
26	chr3:116353400-116354200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr3:116353600-116353800	Active TSS	Brain Cingulate Gyrus	brain
28	chr3:116353600-116354000	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr3:116353600-116354000	Active TSS	Brain Substantia Nigra	brain
30	chr3:116353600-116354200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr3:116353600-116354200	Active TSS	Brain Anterior Caudate	brain
32	chr3:116353800-116354000	Flanking Active TSS	Brain Cingulate Gyrus	brain
33	chr3:116359000-116359800	Enhancers	Adipose Nuclei	Adipose
34	chr3:116359200-116359800	Enhancers	Fetal Brain Male	brain
35	chr3:116359800-116361400	Weak transcription	Fetal Brain Male	brain
36	chr3:116361400-116362400	Enhancers	Fetal Brain Male	brain
37	chr3:116362400-116368000	Weak transcription	Fetal Brain Male	brain
38	chr3:116367000-116368800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr3:116367200-116368000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr3:116367800-116368400	Enhancers	NHEK	skin
41	chr3:116368000-116368400	Enhancers	Fetal Brain Male	brain
42	chr3:116368000-116370200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr3:116368800-116371400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr3:116370000-116370600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr3:116370200-116370400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr3:116371400-116371600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr3:116371600-116379200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr3:116373400-116373800	Enhancers	Brain Cingulate Gyrus	brain
49	chr3:116373400-116373800	Enhancers	Brain Hippocampus Middle	brain
50	chr3:116379200-116380800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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