Variant report

Variant	nsv902431
Chromosome Location	chr14:105587644-105685865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2947)
CpG islands
(count:6171)
Chromatin interactive
region (count:216)
LncRNA
region (count:4)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:2947 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105646970-105647099	K562	blood:	n/a	n/a
2	ARID3A	chr14:105635551-105635751	K562	blood:	n/a	n/a
3	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
4	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
5	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
6	ATF3	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
7	ATF3	chr14:105665582-105665772	K562	blood:	n/a	n/a
8	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:105662435-105662753	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:105669384-105669662	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr14:105663077-105663199	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr14:105667847-105668627	A549	lung:	n/a	chr14:105667887-105667896 chr14:105668189-105668198 chr14:105667888-105667897
16	BCL3	chr14:105681691-105682038	GM12878	blood:	n/a	n/a
17	BCL3	chr14:105668099-105668659	A549	lung:	n/a	chr14:105668189-105668198
18	BCL3	chr14:105670617-105671440	A549	lung:	n/a	n/a
19	BCL3	chr14:105681677-105681921	GM12878	blood:	n/a	n/a
20	BCL3	chr14:105669015-105669647	A549	lung:	n/a	n/a
21	BCL3	chr14:105668932-105669779	A549	lung:	n/a	n/a
22	BHLHE40	chr14:105670862-105671194	HepG2	liver:	n/a	n/a
23	BHLHE40	chr14:105673381-105673508	K562	blood:	n/a	n/a
24	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
25	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
26	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
27	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
28	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
29	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
30	BRCA1	chr14:105663594-105663903	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr14:105607430-105607762	K562	blood:	n/a	n/a
32	CBX3	chr14:105597490-105598063	HCT-116	colon:	n/a	n/a
33	CBX3	chr14:105606276-105606713	K562	blood:	n/a	n/a
34	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
35	CBX3	chr14:105597533-105598007	HCT-116	colon:	n/a	n/a
36	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
37	CBX3	chr14:105665434-105665804	K562	blood:	n/a	n/a
38	CBX3	chr14:105606324-105606692	K562	blood:	n/a	n/a
39	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
40	CCNT2	chr14:105665556-105665715	K562	blood:	n/a	n/a
41	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
42	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
43	CCNT2	chr14:105672167-105672351	K562	blood:	n/a	n/a
44	CCNT2	chr14:105673513-105673600	K562	blood:	n/a	n/a
45	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
46	CCNT2	chr14:105662979-105663291	K562	blood:	n/a	n/a
47	CEBPB	chr14:105602082-105602324	Hela-S3	cervix:	n/a	chr14:105602218-105602229
48	CEBPB	chr14:105602202-105602233	H1-hESC	embryonic stem cell:	n/a	chr14:105602218-105602229
49	CEBPB	chr14:105669556-105669564	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:105602049-105602403	IMR90	lung:	n/a	chr14:105602218-105602229

(count:6171 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105609411-105609461	HNPCEpiC	eye:	n/a
2	chr14:105603153-105603203	HUVEC	blood vessel:	n/a
3	chr14:105659807-105659857	NT2-D1	testis:	n/a
4	chr14:105663019-105663069	H1-hESC	embryonic stem cell:	embryo
5	chr14:105617575-105617625	HCF	heart:	n/a
6	chr14:105659225-105659275	NT2-D1	testis:	n/a
7	chr14:105635706-105635756	HRE	kidney:	n/a
8	chr14:105647510-105647560	GM12878	blood:	n/a
9	chr14:105603389-105603439	AoSMC	blood vessel:	n/a
10	chr14:105663019-105663069	PFSK-1	brain:	n/a
11	chr14:105609411-105609461	HNPCEpiC	eye:	n/a
12	chr14:105603153-105603203	HUVEC	blood vessel:	n/a
13	chr14:105659807-105659857	NT2-D1	testis:	n/a
14	chr14:105663019-105663069	H1-hESC	embryonic stem cell:	embryo
15	chr14:105617575-105617625	HCF	heart:	n/a
16	chr14:105659225-105659275	NT2-D1	testis:	n/a
17	chr14:105635706-105635756	HRE	kidney:	n/a
18	chr14:105647510-105647560	GM12878	blood:	n/a
19	chr14:105603389-105603439	AoSMC	blood vessel:	n/a
20	chr14:105663019-105663069	PFSK-1	brain:	n/a
21	chr14:105670754-105670804	AG10803	skin:	n/a
22	chr14:105617173-105617223	HRPEpiC	eye:	n/a
23	chr14:105625577-105625627	NT2-D1	testis:	n/a
24	chr14:105662805-105662855	A549	lung:	n/a
25	chr14:105615401-105615451	HIPEpiC	eye:	n/a
26	chr14:105643522-105643572	Jurkat	blood:	n/a
27	chr14:105622992-105623042	LNCaP	prostate:	n/a
28	chr14:105683798-105683848	SKMC	muscle:	n/a
29	chr14:105618482-105618532	GM12878	blood:	n/a
30	chr14:105600994-105601044	PANC-1	pancreas:	n/a
31	chr14:105663019-105663069	IMR90	lung:	fetal
32	chr14:105619511-105619561	PrEC	prostate:	n/a
33	chr14:105648697-105648747	GM12892	blood:	n/a
34	chr14:105648024-105648074	SK-N-SH_RA	brain:	n/a
35	chr14:105685075-105685125	NHBE	bronchial:	n/a
36	chr14:105614552-105614602	ovcar-3	ovarian:	n/a
37	chr14:105603153-105603203	A549	lung:	n/a
38	chr14:105608973-105609023	MCF-7	breast:	n/a
39	chr14:105648224-105648274	GM19239	blood:	n/a
40	chr14:105659807-105659857	SKMC	muscle:	n/a
41	chr14:105609472-105609522	H1-hESC	embryonic stem cell:	embryo
42	chr14:105635239-105635289	SK-N-MC	brain:	n/a
43	chr14:105658949-105658999	HEEpiC	esophagus:	n/a
44	chr14:105620358-105620408	AoSMC	blood vessel:	n/a
45	chr14:105612130-105612180	U87	brain:	n/a
46	chr14:105658685-105658735	HRPEpiC	eye:	n/a
47	chr14:105620358-105620408	AG10803	skin:	n/a
48	chr14:105608567-105608617	AG10803	skin:	n/a
49	chr14:105608474-105608524	CMK	blood:	n/a
50	chr14:105647507-105647557	GM19239	blood:	n/a

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
2	chr14:105670960..105673149-chr14:105739734..105742723,2	MCF-7	breast:
3	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:
4	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
5	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
6	chr14:105433467..105435387-chr14:105640925..105642715,2	MCF-7	breast:
7	chr14:105634437..105636135-chr14:105677928..105679697,2	MCF-7	breast:
8	chr14:105635176..105636125-chr14:105747875..105748809,5	K562	blood:
9	chr14:105667147..105672450-chr14:105672961..105678949,7	MCF-7	breast:
10	chr14:105667415..105668351-chr14:105734005..105734857,2	MCF-7	breast:
11	chr14:105557231..105560297-chr14:105661772..105664149,3	MCF-7	breast:
12	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
13	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
14	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
15	chr14:105655523..105657045-chr14:105657884..105660647,2	MCF-7	breast:
16	chr14:105649547..105651849-chr14:105660128..105661657,2	MCF-7	breast:
17	chr14:105667669..105672140-chr14:105712867..105716210,4	MCF-7	breast:
18	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
19	chr14:105585474..105587655-chr14:105643859..105645608,2	MCF-7	breast:
20	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
21	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
22	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
23	chr14:105678829..105680411-chr14:105684341..105687261,3	MCF-7	breast:
24	chr14:105606160..105607990-chr14:105612669..105614397,2	MCF-7	breast:
25	chr14:105486956..105489375-chr14:105652100..105655755,4	MCF-7	breast:
26	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
27	chr14:105670122..105672901-chr14:105693966..105695750,2	K562	blood:
28	chr14:105667108..105669624-chr14:105818365..105820045,2	K562	blood:
29	chr14:105668626..105670243-chr14:105732918..105735863,2	MCF-7	breast:
30	chr14:105636616..105638377-chr14:105781844..105784159,2	K562	blood:
31	chr14:105512170..105512763-chr14:105653793..105654556,2	MCF-7	breast:
32	chr14:105670331..105671987-chr14:105672268..105674643,2	K562	blood:
33	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
34	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
35	chr14:105640130..105641650-chr6:31587480..31589137,3	K562	blood:
36	chr14:105646891..105649186-chr14:105658307..105661126,2	MCF-7	breast:
37	chr14:105673659..105676252-chr14:105822544..105825252,2	K562	blood:
38	chr14:105663948..105665922-chr14:105668555..105670749,2	MCF-7	breast:
39	chr14:105552235..105554666-chr14:105628025..105629965,2	MCF-7	breast:
40	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
41	chr14:105670331..105671987-chr14:105672268..105674643,2	K562	blood:
42	chr14:105557263..105559202-chr14:105649515..105651192,2	MCF-7	breast:
43	chr14:105682211..105684471-chr14:105686659..105689301,2	K562	blood:
44	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
45	chr14:105658555..105662273-chr14:105665604..105667749,3	K562	blood:
46	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
47	chr14:105603768..105606019-chr14:105630363..105631971,2	K562	blood:
48	chr14:105660777..105662281-chr14:105668696..105670709,2	K562	blood:
49	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
50	chr14:105668897..105669930-chr14:105818302..105819064,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1
2	lnc-BTBD6-3	chr14:105681490-105682260	NONHSAT040337
3	lnc-BTBD6-1	chr14:105639541-105639584	ENSG00000257816.1
4	lnc-BTBD6-3	chr14:105682370-105682401	NONHSAT040337

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430

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

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

Variant related genes	Relation type
BRF1	TF binding region
NUDT14	TF binding region
JAG2	TF binding region
ENSG00000257622	TF binding region
BRF1	CpG island
NUDT14	CpG island
JAG2	CpG island
ENSG00000257622	CpG island
ENSG00000183828	chromatin interactions
ENSG00000170027	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000256498	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000182979	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000257622	chromatin interactions

Extended variants
information (count: 4216 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:4216 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11160835	chr14:105587644-105587645	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs28626414	chr14:105587664-105587665	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs137960576	chr14:105587715-105587716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587678450	chr14:105587757-105587758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587729881	chr14:105587852-105587853	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs149467980	chr14:105587902-105587903	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs143869723	chr14:105587903-105587904	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs374049097	chr14:105587932-105587933	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs587722991	chr14:105587944-105587945	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs77902147	chr14:105587948-105587949	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs191598001	chr14:105587974-105587975	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs113204491	chr14:105588049-105588050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs587609411	chr14:105588065-105588066	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs73369116	chr14:105588148-105588149	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs376739761	chr14:105588154-105588155	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs114544339	chr14:105588191-105588192	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs587615653	chr14:105588235-105588236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78485406	chr14:105588295-105588296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188633117	chr14:105588387-105588388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587659891	chr14:105588393-105588394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371337762	chr14:105588410-105588411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs193161122	chr14:105588414-105588415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587747453	chr14:105588452-105588453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587643633	chr14:105588462-105588463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374280469	chr14:105588484-105588485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148592423	chr14:105588516-105588517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117247650	chr14:105588521-105588522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35017361	chr14:105588555-105588556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587651765	chr14:105588566-105588567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587688158	chr14:105588615-105588616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116662293	chr14:105588716-105588717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77475659	chr14:105588722-105588723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587638310	chr14:105588774-105588775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185699907	chr14:105588799-105588800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115989836	chr14:105588854-105588855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189308561	chr14:105588867-105588868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368741026	chr14:105588884-105588885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4267251	chr14:105588928-105588929	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs80326759	chr14:105589031-105589032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12432239	chr14:105589032-105589033	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs587661039	chr14:105589051-105589052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144078069	chr14:105589105-105589106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147316696	chr14:105589112-105589113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180932448	chr14:105589141-105589142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183687711	chr14:105589215-105589216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140942982	chr14:105589223-105589224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587696803	chr14:105589238-105589239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188805932	chr14:105589244-105589245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587651979	chr14:105589257-105589258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587683369	chr14:105589371-105589372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:3132 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105583200-105588000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr14:105586800-105587800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:105587800-105588200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:105588000-105592800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr14:105589000-105590400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:105589200-105590400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr14:105589400-105590000	Enhancers	Duodenum Mucosa	Duodenum
8	chr14:105589800-105590800	Enhancers	Fetal Brain Male	brain
9	chr14:105590000-105590400	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr14:105590000-105590800	Flanking Active TSS	Duodenum Mucosa	Duodenum
11	chr14:105590200-105590600	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr14:105590200-105591200	Enhancers	Colonic Mucosa	Colon
13	chr14:105590400-105591000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
14	chr14:105590400-105602600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:105590600-105591800	Enhancers	Primary hematopoietic stem cells	blood
16	chr14:105590800-105591000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr14:105590800-105591000	Enhancers	Duodenum Mucosa	Duodenum
18	chr14:105590800-105591200	Bivalent Enhancer	HepG2	liver
19	chr14:105590800-105591400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr14:105590800-105591400	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr14:105590800-105591400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr14:105590800-105591400	Enhancers	Placenta	Placenta
23	chr14:105590800-105591600	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr14:105590800-105593000	Enhancers	Fetal Intestine Large	intestine
25	chr14:105591000-105591200	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr14:105591000-105591200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
27	chr14:105591000-105591200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
28	chr14:105591000-105591400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
29	chr14:105591000-105591400	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr14:105591000-105591600	Enhancers	Primary T cells from cord blood	blood
31	chr14:105591000-105591600	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr14:105591000-105591600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:105591200-105591400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr14:105591200-105591400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
35	chr14:105591200-105591400	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr14:105591200-105591400	Bivalent Enhancer	HSMMtube	muscle
37	chr14:105591200-105591600	Enhancers	Fetal Thymus	thymus
38	chr14:105591200-105592000	Enhancers	Fetal Intestine Small	intestine
39	chr14:105591400-105591600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
40	chr14:105591400-105591600	Bivalent Enhancer	HepG2	liver
41	chr14:105591400-105591800	Enhancers	Duodenum Mucosa	Duodenum
42	chr14:105591800-105592200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr14:105592200-105593400	Enhancers	Duodenum Mucosa	Duodenum
44	chr14:105592400-105593200	Enhancers	Esophagus	oesophagus
45	chr14:105592600-105593600	Enhancers	Fetal Intestine Small	intestine
46	chr14:105592600-105593800	Bivalent Enhancer	HepG2	liver
47	chr14:105592800-105593400	Enhancers	Brain Germinal Matrix	brain
48	chr14:105592800-105593600	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr14:105592800-105593600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr14:105593000-105593200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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