Variant report

Variant	nsv1042294
Chromosome Location	chr14:34974774-35017859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:551)
Chromatin interactive
region (count:69)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35008603-35009026	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:34975027-34975388	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:34976759-34976917	HepG2	liver:	n/a	n/a
4	ATF1	chr14:35008732-35009086	K562	blood:	n/a	n/a
5	ATF2	chr14:35008667-35009076	GM12878	blood:	n/a	n/a
6	BACH1	chr14:35008433-35008921	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:35015666-35017003	GM12878	blood:	n/a	n/a
8	BATF	chr14:35015746-35016579	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:35015741-35017025	GM12878	blood:	n/a	chr14:35016380-35016389
10	BCL11A	chr14:35015736-35017033	GM12878	blood:	n/a	chr14:35016380-35016389
11	BCL11A	chr14:35014970-35015263	GM12878	blood:	n/a	n/a
12	BCL3	chr14:35008651-35009057	A549	lung:	n/a	chr14:35008924-35008933 chr14:35009006-35009015
13	BCLAF1	chr14:35008564-35009019	GM12878	blood:	n/a	chr14:35008924-35008933 chr14:35009006-35009015
14	BHLHE40	chr14:35014883-35015262	HepG2	liver:	n/a	n/a
15	BHLHE40	chr14:35008534-35008944	K562	blood:	n/a	n/a
16	BHLHE40	chr14:35008473-35009036	HepG2	liver:	n/a	n/a
17	BHLHE40	chr14:35015741-35016651	HepG2	liver:	n/a	chr14:35016542-35016558 chr14:35016563-35016579
18	BRCA1	chr14:35008677-35009053	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr14:35008514-35008984	HepG2	liver:	n/a	n/a
20	CBX3	chr14:35015658-35016767	K562	blood:	n/a	n/a
21	CBX3	chr14:35008623-35009009	K562	blood:	n/a	n/a
22	CBX3	chr14:35015762-35016560	K562	blood:	n/a	n/a
23	CCNT2	chr14:35008609-35009081	K562	blood:	n/a	chr14:35009026-35009035
24	CEBPB	chr14:35015734-35016767	K562	blood:	n/a	n/a
25	CEBPB	chr14:35008708-35009013	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:35008772-35008834	K562	blood:	n/a	n/a
27	CEBPB	chr14:35008731-35009055	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:35008792-35008986	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:34983120-34983159	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:35015820-35016539	GM12878	blood:	n/a	n/a
31	CEBPB	chr14:35015644-35016790	GM12878	blood:	n/a	n/a
32	CEBPB	chr14:34989102-34989228	HepG2	liver:	n/a	chr14:34989146-34989157
33	CEBPB	chr14:34983093-34983266	K562	blood:	n/a	n/a
34	CEBPB	chr14:34975538-34975797	HepG2	liver:	n/a	chr14:34975643-34975654
35	CEBPB	chr14:35008703-35008999	HepG2	liver:	n/a	n/a
36	CEBPB	chr14:35015820-35016202	K562	blood:	n/a	n/a
37	CEBPB	chr14:34976909-34976949	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:35017116-35017444	K562	blood:	n/a	n/a
39	CEBPB	chr14:34989112-34989177	A549	lung:	n/a	chr14:34989146-34989157
40	CEBPD	chr14:35008579-35009057	HepG2	liver:	n/a	n/a
41	CEBPD	chr14:35008432-35009048	HepG2	liver:	n/a	n/a
42	CEBPD	chr14:35015499-35016794	K562	blood:	n/a	n/a
43	CEBPD	chr14:34993437-34993770	K562	blood:	n/a	n/a
44	CHD1	chr14:35007665-35009150	IMR90	lung:	n/a	chr14:35008580-35008590
45	CHD1	chr14:35007894-35008967	GM12878	blood:	n/a	chr14:35008580-35008590
46	CHD1	chr14:35008083-35008889	H1-hESC	embryonic stem cell:	n/a	chr14:35008580-35008590
47	CHD2	chr14:35008676-35009100	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr14:35008538-35008883	K562	blood:	n/a	chr14:35008580-35008590
49	CHD2	chr14:35008630-35009025	GM12878	blood:	n/a	n/a
50	CHD2	chr14:35008567-35009013	HepG2	liver:	n/a	chr14:35008580-35008590

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35009852-35009902	NHDF-neo	bronchial:	n/a
2	chr14:35008877-35008927	HRE	kidney:	n/a
3	chr14:35009852-35009902	NHDF-neo	bronchial:	n/a
4	chr14:35008877-35008927	HRE	kidney:	n/a
5	chr14:35008877-35008927	AG04450	lung:	fetal
6	chr14:35008500-35008550	PrEC	prostate:	n/a
7	chr14:35006074-35006124	NH-A	brain:	n/a
8	chr14:35008750-35008800	HRPEpiC	eye:	n/a
9	chr14:35008877-35008927	GM12891	blood:	n/a
10	chr14:35008877-35008927	SKMC	muscle:	n/a
11	chr14:35006074-35006124	ProgFib	skin:	n/a
12	chr14:35008500-35008550	NH-A	brain:	n/a
13	chr14:35017319-35017369	Caco-2	colon:	n/a
14	chr14:35008750-35008800	BE2_C	brain:	n/a
15	chr14:35009852-35009902	AG09309	skin:	n/a
16	chr14:35009492-35009542	RPTEC	kidney:	n/a
17	chr14:35017319-35017369	SAEC	small airway:	n/a
18	chr14:35006074-35006124	HMEC	breast:	n/a
19	chr14:35008750-35008800	LNCaP	prostate:	n/a
20	chr14:35006074-35006124	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:35008857-35008907	NB4	blood:	n/a
22	chr14:35008661-35008711	NH-A	brain:	n/a
23	chr14:35009492-35009542	K562	blood:	n/a
24	chr14:35008661-35008711	ECC-1	luminal epithelium:	n/a
25	chr14:35017319-35017369	MCF-7	breast:	n/a
26	chr14:35008661-35008711	HCT-116	colon:	n/a
27	chr14:35008661-35008711	Jurkat	blood:	n/a
28	chr14:35009852-35009902	HCF	heart:	n/a
29	chr14:35008661-35008711	ProgFib	skin:	n/a
30	chr14:35008857-35008907	BE2_C	brain:	n/a
31	chr14:35009492-35009542	NH-A	brain:	n/a
32	chr14:35008500-35008550	NB4	blood:	n/a
33	chr14:35006074-35006124	SAEC	small airway:	n/a
34	chr14:35008877-35008927	HCM	heart:	n/a
35	chr14:35006074-35006124	NHBE	bronchial:	n/a
36	chr14:35008877-35008927	HRPEpiC	eye:	n/a
37	chr14:35008661-35008711	MCF-7	breast:	n/a
38	chr14:35008750-35008800	HCF	heart:	n/a
39	chr14:35017319-35017369	HCPEpiC	choroid plexus:	n/a
40	chr14:35006074-35006124	HCT-116	colon:	n/a
41	chr14:35009852-35009902	MCF-7	breast:	n/a
42	chr14:35008661-35008711	T-47D	breast:	n/a
43	chr14:35009852-35009902	GM19239	blood:	n/a
44	chr14:35008750-35008800	PFSK-1	brain:	n/a
45	chr14:35008857-35008907	BJ	skin:	n/a
46	chr14:35008877-35008927	GM12878	blood:	n/a
47	chr14:35008877-35008927	AG09319	gingival:	n/a
48	chr14:35009492-35009542	LNCaP	prostate:	n/a
49	chr14:35009852-35009902	SK-N-SH_RA	brain:	n/a
50	chr14:35008857-35008907	AG04450	lung:	fetal

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35003178..35006952-chr14:35007318..35009026,4	MCF-7	breast:
2	chr14:34797417..34799654-chr14:35017218..35018796,2	K562	blood:
3	chr14:34964955..34967907-chr14:34973617..34975342,2	MCF-7	breast:
4	chr14:34929449..34931749-chr14:34993451..34995469,2	MCF-7	breast:
5	chr14:35016499..35019288-chr14:35182699..35184219,2	MCF-7	breast:
6	chr14:34988212..34991745-chr14:34992465..34994604,3	MCF-7	breast:
7	chr1:231188613..231189133-chr14:35017234..35017819,2	MCF-7	breast:
8	chr14:34987498..34989819-chr14:35007397..35008989,2	MCF-7	breast:
9	chr14:35000955..35003897-chr14:35015691..35017291,2	MCF-7	breast:
10	chr14:35009037..35010904-chr14:35021766..35024411,2	K562	blood:
11	chr14:35017489..35019232-chr14:35116363..35118749,2	MCF-7	breast:
12	chr1:149223853..149225389-chr14:35015592..35017210,2	MCF-7	breast:
13	chr14:34988212..34991745-chr14:34992465..34994604,3	MCF-7	breast:
14	chr14:34992410..34994552-chr14:35006648..35008744,2	MCF-7	breast:
15	chr14:34929804..34932141-chr14:35000832..35004516,3	K562	blood:
16	chr14:35005592..35010362-chr14:35016916..35020262,4	K562	blood:
17	chr14:34997979..35000890-chr14:35004002..35008014,4	K562	blood:
18	chr14:35016452..35018611-chr14:35133910..35135545,2	K562	blood:
19	chr14:34993830..34996289-chr14:35004002..35006048,2	K562	blood:
20	chr14:34995358..34997093-chr14:35024116..35025822,2	K562	blood:
21	chr14:34931690..34933656-chr14:35005412..35007221,2	K562	blood:
22	chr14:34980447..34984280-chr14:35015816..35019856,3	MCF-7	breast:
23	chr14:34997304..35000255-chr14:35008172..35010280,2	K562	blood:
24	chr14:35016252..35019435-chr14:35175626..35179365,3	MCF-7	breast:
25	chr14:35005764..35008884-chr14:35021719..35025749,6	K562	blood:
26	chr14:35004626..35011116-chr14:35015634..35020787,10	MCF-7	breast:
27	chr14:35005104..35007114-chr14:35007414..35009874,3	K562	blood:
28	chr14:34792427..34794155-chr14:35007082..35008607,2	MCF-7	breast:
29	chr14:35002309..35005186-chr14:35018776..35021150,2	MCF-7	breast:
30	chr14:35016883..35018423-chr14:35574764..35577501,2	MCF-7	breast:
31	chr14:34990714..34993643-chr14:35006292..35008810,2	K562	blood:
32	chr14:34990714..34993643-chr14:35006292..35008810,2	K562	blood:
33	chr14:35017271..35020208-chr14:35082278..35083991,2	MCF-7	breast:
34	chr14:35015757..35018418-chr4:39977549..39979834,2	MCF-7	breast:
35	chr14:34996976..35002931-chr14:35005430..35010920,7	MCF-7	breast:
36	chr14:35003178..35006952-chr14:35007318..35009026,4	MCF-7	breast:
37	chr14:34998512..35003069-chr14:35021669..35025917,5	MCF-7	breast:
38	chr14:35007550..35010317-chr14:35342022..35344512,2	K562	blood:
39	chr14:35005506..35011243-chr14:35020994..35025666,12	MCF-7	breast:
40	chr14:35007550..35010391-chr14:35343012..35345148,2	K562	blood:
41	chr14:35008040..35009005-chr16:27214684..27215320,2	Hela-S3	cervix:
42	chr14:35001326..35003361-chr14:35005467..35007300,3	K562	blood:
43	chr14:35017186..35019068-chr14:35256724..35258976,2	MCF-7	breast:
44	chr14:35007630..35008465-chr16:73238858..73239382,2	MCF-7	breast:
45	chr14:34985976..34987931-chr14:35007272..35009359,2	MCF-7	breast:
46	chr14:35016160..35018954-chr14:35320492..35322117,2	MCF-7	breast:
47	chr14:35004626..35011116-chr14:35015634..35020787,10	MCF-7	breast:
48	chr14:34933163..34934738-chr14:35003028..35005166,2	K562	blood:
49	chr14:34990134..34992154-chr14:35005229..35008582,3	MCF-7	breast:
50	chr14:34929666..34933656-chr14:35005721..35010391,9	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EAPP-1	chr14:35011288-35011650	ENSG00000259002.1
2	lnc-EAPP-2	chr14:35013705-35013999	ENSG00000258612.1
3	lnc-EAPP-1	chr14:35011023-35011204	ENSG00000259002.1
4	lnc-EAPP-2	chr14:35015063-35015183	ENSG00000258612.1

No data

Variant related genes	Relation type
EAPP	TF binding region
ENSG00000259002	TF binding region
RNU1-27P	TF binding region
ENSG00000258612	TF binding region
EAPP	CpG island
ENSG00000259002	CpG island
RNU1-27P	CpG island
ENSG00000258612	CpG island
ENSG00000129518	chromatin interactions
ENSG00000206588	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000164253	chromatin interactions
ENSG00000165389	chromatin interactions
ENSG00000165410	chromatin interactions
ENSG00000129521	chromatin interactions
ENSG00000107816	chromatin interactions
ENSG00000121892	chromatin interactions
ENSG00000025039	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000206596	chromatin interactions
ENSG00000155666	chromatin interactions

Extended variants
information (count: 1396 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193192913	chr14:34974838-34974839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549622721	chr14:34974867-34974868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529039595	chr14:34974891-34974892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549262218	chr14:34974928-34974929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562635764	chr14:34974929-34974930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199567391	chr14:34974953-34974954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545121206	chr14:34975010-34975011	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs557580141	chr14:34975034-34975035	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs78582324	chr14:34975049-34975050	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs377647151	chr14:34975246-34975247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183250780	chr14:34975282-34975283	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs111650715	chr14:34975356-34975357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs572601961	chr14:34975367-34975368	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs534312724	chr14:34975382-34975383	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs547542403	chr14:34975413-34975414	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs375918202	chr14:34975448-34975449	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs7155698	chr14:34975483-34975484	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556862905	chr14:34975507-34975508	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187176861	chr14:34975512-34975513	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs537483218	chr14:34975514-34975515	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs557352646	chr14:34975541-34975542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs577181771	chr14:34975580-34975581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs561295116	chr14:34975586-34975587	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs540332351	chr14:34975636-34975637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559944251	chr14:34975638-34975639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201313579	chr14:34975788-34975789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111270285	chr14:34975790-34975791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191672551	chr14:34975800-34975801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562803232	chr14:34975815-34975816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11156846	chr14:34975884-34975885	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs551675120	chr14:34975914-34975915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116835991	chr14:34975922-34975923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527649615	chr14:34975923-34975924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146441303	chr14:34975935-34975936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139873541	chr14:34975937-34975938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536891014	chr14:34975945-34975946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550093792	chr14:34975962-34975963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527646623	chr14:34975993-34975994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570042957	chr14:34976012-34976013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184113441	chr14:34976019-34976020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61981517	chr14:34976020-34976021	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs4982186	chr14:34976028-34976029	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs570914460	chr14:34976073-34976074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533549535	chr14:34976115-34976116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553870309	chr14:34976131-34976132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573636706	chr14:34976149-34976150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151139436	chr14:34976150-34976151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556413918	chr14:34976196-34976197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565877715	chr14:34976211-34976212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369384232	chr14:34976219-34976220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:34966400-34985400	Weak transcription	Primary B cells from cord blood	blood
2	chr14:34967000-34985200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:34967000-34985200	Weak transcription	Fetal Lung	lung
4	chr14:34967600-34985200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr14:34967800-34984800	Weak transcription	Fetal Stomach	stomach
6	chr14:34968400-34975200	Weak transcription	Stomach Mucosa	stomach
7	chr14:34968400-34984800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr14:34969800-34974800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr14:34971000-34986000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr14:34971800-34985000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr14:34972200-34975000	Weak transcription	A549	lung
12	chr14:34972200-34975800	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr14:34972200-34984400	Weak transcription	Fetal Muscle Leg	muscle
14	chr14:34972200-34984800	Weak transcription	Ovary	ovary
15	chr14:34972200-34989800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr14:34972600-34985000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:34972800-34984800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr14:34972800-34985000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:34972800-34986000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:34974200-34976400	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr14:34974400-34975000	Enhancers	HepG2	liver
22	chr14:34974400-34976800	Enhancers	Fetal Intestine Large	intestine
23	chr14:34974600-34976200	Enhancers	Fetal Intestine Small	intestine
24	chr14:34974600-34985000	Weak transcription	Primary B cells from peripheral blood	blood
25	chr14:34974800-34975600	Enhancers	Pancreas	Pancrea
26	chr14:34974800-34976000	Enhancers	Duodenum Mucosa	Duodenum
27	chr14:34975000-34975600	Enhancers	A549	lung
28	chr14:34975000-34975600	Flanking Active TSS	HepG2	liver
29	chr14:34975000-34975600	Enhancers	K562	blood
30	chr14:34975200-34975600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:34975200-34975600	Enhancers	Gastric	stomach
32	chr14:34975200-34975600	Enhancers	Stomach Mucosa	stomach
33	chr14:34975600-34977400	Enhancers	HepG2	liver
34	chr14:34975600-34985000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr14:34975600-34988000	Weak transcription	A549	lung
36	chr14:34975600-34988200	Weak transcription	Gastric	stomach
37	chr14:34975600-34989800	Weak transcription	Pancreas	Pancrea
38	chr14:34975800-34976200	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr14:34976000-34985000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr14:34976200-34984400	Weak transcription	Fetal Intestine Small	intestine
41	chr14:34976200-34984800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr14:34976400-34976800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr14:34976800-34977000	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr14:34976800-34984800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:34976800-34984800	Weak transcription	Fetal Intestine Large	intestine
46	chr14:34977000-34984800	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr14:34977200-34977400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:34977400-34985000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:34977400-34985000	Weak transcription	HepG2	liver
50	chr14:34978600-34985200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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