Variant report

Variant	nsv566153
Chromosome Location	chr14:105574843-105617042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:287)
CpG islands
(count:1955)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr14:105597533-105598007	HCT-116	colon:	n/a	n/a
2	CBX3	chr14:105606324-105606692	K562	blood:	n/a	n/a
3	CBX3	chr14:105606276-105606713	K562	blood:	n/a	n/a
4	CBX3	chr14:105607430-105607762	K562	blood:	n/a	n/a
5	CBX3	chr14:105597490-105598063	HCT-116	colon:	n/a	n/a
6	CEBPB	chr14:105602051-105602404	K562	blood:	n/a	chr14:105602218-105602229
7	CEBPB	chr14:105574845-105575152	A549	lung:	n/a	chr14:105574978-105574989
8	CEBPB	chr14:105574819-105575115	HepG2	liver:	n/a	chr14:105574978-105574989
9	CEBPB	chr14:105602202-105602233	H1-hESC	embryonic stem cell:	n/a	chr14:105602218-105602229
10	CEBPB	chr14:105574958-105575149	H1-hESC	embryonic stem cell:	n/a	chr14:105574978-105574989
11	CEBPB	chr14:105585012-105585717	MCF-7	breast:	n/a	n/a
12	CEBPB	chr14:105602082-105602324	Hela-S3	cervix:	n/a	chr14:105602218-105602229
13	CEBPB	chr14:105602070-105602404	HepG2	liver:	n/a	chr14:105602218-105602229
14	CEBPB	chr14:105585152-105585236	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:105584857-105585623	MCF-7	breast:	n/a	n/a
16	CEBPB	chr14:105602145-105602475	MCF-7	breast:	n/a	chr14:105602218-105602229
17	CEBPB	chr14:105602053-105602402	A549	lung:	n/a	chr14:105602218-105602229
18	CEBPB	chr14:105602020-105602475	A549	lung:	n/a	chr14:105602218-105602229
19	CEBPB	chr14:105602049-105602403	IMR90	lung:	n/a	chr14:105602218-105602229
20	CREB1	chr14:105603330-105603686	K562	blood:	n/a	n/a
21	CTCF	chr14:105611604-105611661	MCF-7	breast:	n/a	chr14:105611619-105611637 chr14:105611626-105611634
22	CTCF	chr14:105585510-105585652	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:105585534-105585613	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:105613155-105613312	GM12878	blood:	n/a	n/a
25	CTCF	chr14:105585980-105586130	SAEC	small airway:	n/a	chr14:105586102-105586115
26	CTCF	chr14:105611480-105611630	GM12870	blood:	n/a	chr14:105611569-105611579
27	CTCF	chr14:105611550-105611694	Hela-S3	cervix:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
28	CTCF	chr14:105585507-105585660	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:105586080-105586230	SAEC	small airway:	n/a	chr14:105586136-105586145 chr14:105586102-105586115
30	CTCF	chr14:105613214-105613323	Fibrobl	skin:	n/a	n/a
31	CTCF	chr14:105586020-105586170	NHEK	skin:	n/a	chr14:105586136-105586145 chr14:105586102-105586115
32	CTCF	chr14:105611580-105611730	GM12878	blood:	n/a	chr14:105611619-105611637 chr14:105611626-105611634
33	CTCF	chr14:105611660-105611810	NB4	blood:	n/a	n/a
34	CTCF	chr14:105611526-105611711	MCF-7	breast:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
35	CTCF	chr14:105585600-105585750	NHEK	skin:	n/a	n/a
36	CTCF	chr14:105611538-105611710	NHEK	skin:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
37	CTCF	chr14:105611600-105611750	SAEC	small airway:	n/a	chr14:105611619-105611637 chr14:105611626-105611634
38	CTCF	chr14:105585940-105586090	NHEK	skin:	n/a	n/a
39	CTCF	chr14:105611600-105611750	Hela-S3	cervix:	n/a	chr14:105611619-105611637 chr14:105611626-105611634
40	CTCF	chr14:105611560-105611710	HCFaa	heart:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
41	CTCF	chr14:105611420-105611570	GM12864	blood:	n/a	n/a
42	CTCF	chr14:105611520-105611670	HCPEpiC	choroid plexus:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
43	CTCF	chr14:105611524-105611706	HepG2	liver:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
44	CTCF	chr14:105613180-105613330	GM12865	blood:	n/a	n/a
45	CTCF	chr14:105611564-105611683	MCF-7	breast:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
46	CTCF	chr14:105613180-105613330	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr14:105585502-105585658	NHEK	skin:	n/a	n/a
48	CTCF	chr14:105611520-105611670	HRPEpiC	eye:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
49	CTCF	chr14:105585547-105585607	LNCaP	prostate:	n/a	n/a
50	CTCF	chr14:105611540-105611690	WERI-Rb-1	eye:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105612753-105612803	CMK	blood:	n/a
2	chr14:105603389-105603439	HAEpiC	amniotic membrane:	n/a
3	chr14:105609831-105609881	GM12892	blood:	n/a
4	chr14:105612753-105612803	CMK	blood:	n/a
5	chr14:105603389-105603439	HAEpiC	amniotic membrane:	n/a
6	chr14:105609831-105609881	GM12892	blood:	n/a
7	chr14:105609411-105609461	MCF-7	breast:	n/a
8	chr14:105608973-105609023	HIPEpiC	eye:	n/a
9	chr14:105582624-105582674	GM19239	blood:	n/a
10	chr14:105608973-105609023	GM06990	blood:	n/a
11	chr14:105609472-105609522	HCT-116	colon:	n/a
12	chr14:105616988-105617038	AG04450	lung:	fetal
13	chr14:105616988-105617038	NHBE	bronchial:	n/a
14	chr14:105612130-105612180	AG04449	skin:	fetal
15	chr14:105608474-105608524	GM06990	blood:	n/a
16	chr14:105576362-105576412	AoSMC	blood vessel:	n/a
17	chr14:105609516-105609566	ECC-1	luminal epithelium:	n/a
18	chr14:105615459-105615509	SKMC	muscle:	n/a
19	chr14:105614564-105614614	HMEC	breast:	n/a
20	chr14:105576362-105576412	HCPEpiC	choroid plexus:	n/a
21	chr14:105609831-105609881	BE2_C	brain:	n/a
22	chr14:105609472-105609522	AG09309	skin:	n/a
23	chr14:105608973-105609023	PANC-1	pancreas:	n/a
24	chr14:105614818-105614868	PANC-1	pancreas:	n/a
25	chr14:105614564-105614614	T-47D	breast:	n/a
26	chr14:105582624-105582674	SK-N-SH	brain:	n/a
27	chr14:105609411-105609461	NH-A	brain:	n/a
28	chr14:105603460-105603510	HCF	heart:	n/a
29	chr14:105608973-105609023	GM12892	blood:	n/a
30	chr14:105616988-105617038	A549	lung:	n/a
31	chr14:105609516-105609566	Hela-S3	cervix:	n/a
32	chr14:105609472-105609522	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:105608474-105608524	HUVEC	blood vessel:	n/a
34	chr14:105603389-105603439	GM12891	blood:	n/a
35	chr14:105612787-105612837	PrEC	prostate:	n/a
36	chr14:105600994-105601044	HRPEpiC	eye:	n/a
37	chr14:105614552-105614602	AG09319	gingival:	n/a
38	chr14:105584462-105584512	SKMC	muscle:	n/a
39	chr14:105612753-105612803	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:105614564-105614614	Jurkat	blood:	n/a
41	chr14:105609411-105609461	GM12878	blood:	n/a
42	chr14:105613102-105613152	ProgFib	skin:	n/a
43	chr14:105605750-105605800	HepG2	liver:	n/a
44	chr14:105614818-105614868	IMR90	lung:	fetal
45	chr14:105613102-105613152	NH-A	brain:	n/a
46	chr14:105608567-105608617	HCF	heart:	n/a
47	chr14:105600994-105601044	GM12878	blood:	n/a
48	chr14:105614552-105614602	HCM	heart:	n/a
49	chr14:105615401-105615451	H1-hESC	embryonic stem cell:	embryo
50	chr14:105576362-105576412	GM12891	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105556860..105558487-chr14:105603973..105605818,2	K562	blood:
2	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
3	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:
4	chr14:105566584..105569448-chr14:105610028..105612847,2	MCF-7	breast:
5	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
6	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
7	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
8	chr14:105438558..105440399-chr14:105616229..105618880,2	MCF-7	breast:
9	chr14:105556660..105559437-chr14:105588253..105590015,2	MCF-7	breast:
10	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
11	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
12	chr14:105567398..105568987-chr14:105582432..105584780,2	MCF-7	breast:
13	chr14:105553187..105555561-chr14:105589136..105591325,2	MCF-7	breast:
14	chr14:105448909..105450840-chr14:105583708..105586505,2	MCF-7	breast:
15	chr14:105567450..105569151-chr14:105572022..105574911,2	K562	blood:
16	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
17	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
18	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
19	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
20	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
21	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
22	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
23	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:
24	chr14:105605014..105607392-chr14:105623375..105626287,2	K562	blood:
25	chr14:105567323..105568937-chr14:105583984..105585803,2	MCF-7	breast:
26	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:
27	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
28	chr14:105606160..105607990-chr14:105612669..105614397,2	MCF-7	breast:
29	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
30	chr14:105605892..105608252-chr14:105621955..105625449,3	K562	blood:
31	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
32	chr14:105601373..105604174-chr14:105610785..105613135,3	MCF-7	breast:
33	chr14:105585474..105587655-chr14:105643859..105645608,2	MCF-7	breast:
34	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
35	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
36	chr14:105601373..105604174-chr14:105610785..105613135,3	MCF-7	breast:
37	chr14:105603768..105606019-chr14:105630363..105631971,2	K562	blood:
38	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
39	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
40	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
41	chr14:105584495..105586972-chr14:105646028..105648252,2	MCF-7	breast:
42	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
43	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	JAG2	hsa-miR-124-3p	chr14:105608233-105608227
2	JAG2	hsa-miR-124-3p	chr14:105608227-105608246

Variant related genes	Relation type
JAG2	TF binding region
ENSG00000258154	TF binding region
JAG2	CpG island
ENSG00000258154	CpG island
ENSG00000184916	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000257622	chromatin interactions

Extended variants
information (count: 1725 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1725 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9324081	chr14:105574843-105574844	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192461308	chr14:105574865-105574866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183928342	chr14:105574889-105574890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188252630	chr14:105574916-105574917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587728825	chr14:105574941-105574942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587627870	chr14:105574962-105574963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587679115	chr14:105574964-105574965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115411082	chr14:105574968-105574969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587611741	chr14:105575033-105575034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373526663	chr14:105575035-105575036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587772258	chr14:105575073-105575074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116715196	chr14:105575105-105575106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375912718	chr14:105575113-105575114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150234841	chr14:105575129-105575130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587764789	chr14:105575147-105575148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10144185	chr14:105575159-105575160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs587719991	chr14:105575163-105575164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7146670	chr14:105575167-105575168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373448419	chr14:105575169-105575170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148954908	chr14:105575204-105575205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143672547	chr14:105575205-105575206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7146692	chr14:105575208-105575209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs143804266	chr14:105575235-105575236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193005994	chr14:105575249-105575250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587602943	chr14:105575252-105575253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587662862	chr14:105575260-105575261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369678961	chr14:105575265-105575266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587619647	chr14:105575266-105575267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587719606	chr14:105575267-105575268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184787569	chr14:105575270-105575271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34437981	chr14:105575272-105575273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11626561	chr14:105575288-105575289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376332554	chr14:105575293-105575294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10144463	chr14:105575294-105575295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs587680188	chr14:105575331-105575332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587754712	chr14:105575337-105575338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587657205	chr14:105575338-105575339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587714233	chr14:105575347-105575348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587769480	chr14:105575348-105575349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587643059	chr14:105575353-105575354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189692918	chr14:105575356-105575357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587742038	chr14:105575368-105575369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75855822	chr14:105575379-105575380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181803779	chr14:105575383-105575384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587708522	chr14:105575450-105575451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587603018	chr14:105575484-105575485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185775736	chr14:105575489-105575490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189456116	chr14:105575511-105575512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587635412	chr14:105575591-105575592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139107676	chr14:105575599-105575600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Breast cancer	22522925	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105574000-105576800	Weak transcription	Right Atrium	heart
2	chr14:105574600-105575000	Enhancers	A549	lung
3	chr14:105576200-105576400	Enhancers	Esophagus	oesophagus
4	chr14:105576400-105581200	Weak transcription	Esophagus	oesophagus
5	chr14:105578400-105578800	Active TSS	HSMM	muscle
6	chr14:105581000-105581800	Enhancers	NHEK	skin
7	chr14:105581200-105582200	Enhancers	Esophagus	oesophagus
8	chr14:105581400-105581800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:105581800-105584600	Weak transcription	NHEK	skin
10	chr14:105581800-105584800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:105582200-105584400	Weak transcription	Esophagus	oesophagus
12	chr14:105582400-105582600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:105583200-105588000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr14:105584400-105585200	Enhancers	Esophagus	oesophagus
15	chr14:105584400-105586800	Enhancers	HMEC	breast
16	chr14:105584600-105585200	Enhancers	Placenta Amnion	Placenta Amnion
17	chr14:105584600-105585600	Enhancers	NHEK	skin
18	chr14:105584600-105586800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr14:105584800-105586400	Enhancers	Placenta	Placenta
20	chr14:105584800-105586400	Enhancers	Fetal Thymus	thymus
21	chr14:105584800-105586800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr14:105584800-105586800	Enhancers	Pancreas	Pancrea
23	chr14:105584800-105587000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:105585000-105585800	Enhancers	Primary hematopoietic stem cells	blood
25	chr14:105585000-105586000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr14:105585000-105586200	Enhancers	Gastric	stomach
27	chr14:105585200-105585600	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr14:105585200-105585800	Weak transcription	Esophagus	oesophagus
29	chr14:105585200-105586200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr14:105585200-105586200	Enhancers	Stomach Mucosa	stomach
31	chr14:105585400-105586400	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr14:105585600-105585800	Bivalent Enhancer	Colonic Mucosa	Colon
33	chr14:105585600-105586000	Flanking Active TSS	NHEK	skin
34	chr14:105585600-105586200	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:105585600-105586400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr14:105585600-105586600	Enhancers	Placenta Amnion	Placenta Amnion
37	chr14:105585800-105586800	Enhancers	Esophagus	oesophagus
38	chr14:105586000-105586200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr14:105586000-105587000	Enhancers	NHEK	skin
40	chr14:105586800-105587800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:105587800-105588200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:105588000-105592800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr14:105589000-105590400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:105589200-105590400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:105589400-105590000	Enhancers	Duodenum Mucosa	Duodenum
46	chr14:105589800-105590800	Enhancers	Fetal Brain Male	brain
47	chr14:105590000-105590400	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr14:105590000-105590800	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr14:105590200-105590600	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr14:105590200-105591200	Enhancers	Colonic Mucosa	Colon

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