Variant report

Variant	esv3405849
Chromosome Location	chr14:71786224-71789072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:802)
CpG islands
(count:489)
Chromatin interactive
region (count:10)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:71787874-71787907	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:71786747-71787215	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:71788588-71789002	HepG2	liver:	n/a	n/a
4	ATF1	chr14:71786899-71787253	K562	blood:	n/a	n/a
5	ATF2	chr14:71786813-71787233	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:71786767-71787272	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr14:71786739-71787483	GM12878	blood:	n/a	n/a
8	ATF2	chr14:71786718-71787308	GM12878	blood:	n/a	n/a
9	ATF3	chr14:71786801-71787120	K562	blood:	n/a	n/a
10	ATF3	chr14:71786897-71787101	K562	blood:	n/a	n/a
11	BACH1	chr14:71786361-71787281	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr14:71787112-71787386	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:71786999-71787439	GM12878	blood:	n/a	chr14:71787286-71787299 chr14:71787358-71787367
14	BCL3	chr14:71786973-71787501	GM12878	blood:	n/a	chr14:71787286-71787299 chr14:71787358-71787367 chr14:71786990-71786999
15	BCL3	chr14:71786608-71787295	A549	lung:	n/a	chr14:71786990-71786999
16	BCLAF1	chr14:71786666-71787488	GM12878	blood:	n/a	chr14:71787286-71787299 chr14:71787358-71787367 chr14:71786990-71786999
17	BCLAF1	chr14:71787552-71788470	GM12878	blood:	n/a	chr14:71787730-71787739 chr14:71788061-71788074
18	BCLAF1	chr14:71787100-71788531	GM12878	blood:	n/a	chr14:71787286-71787299 chr14:71787358-71787367 chr14:71787730-71787739 chr14:71788061-71788074
19	BHLHE40	chr14:71787745-71787945	K562	blood:	n/a	n/a
20	BHLHE40	chr14:71786754-71787454	K562	blood:	n/a	n/a
21	BHLHE40	chr14:71786794-71787469	GM12878	blood:	n/a	n/a
22	BRCA1	chr14:71786690-71787255	HepG2	liver:	n/a	chr14:71787028-71787037
23	BRCA1	chr14:71786751-71787315	GM12878	blood:	n/a	chr14:71787028-71787037
24	BRCA1	chr14:71786637-71787379	Hela-S3	cervix:	n/a	chr14:71787028-71787037
25	BRCA1	chr14:71787754-71787951	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr14:71786666-71787220	H1-hESC	embryonic stem cell:	n/a	chr14:71787028-71787037
27	CBX3	chr14:71787031-71787329	K562	blood:	n/a	n/a
28	CCNT2	chr14:71786795-71788289	K562	blood:	n/a	chr14:71787977-71787986 chr14:71787390-71787399
29	CEBPB	chr14:71788387-71789078	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr14:71788644-71789094	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr14:71788110-71789106	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr14:71788542-71789085	MCF-7	breast:	n/a	n/a
33	CEBPB	chr14:71788734-71789026	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:71786810-71787336	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:71788493-71789056	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPD	chr14:71787079-71787535	HepG2	liver:	n/a	n/a
37	CHD1	chr14:71787736-71789103	H1-hESC	embryonic stem cell:	n/a	chr14:71787925-71787935
38	CHD1	chr14:71786647-71788521	GM12878	blood:	n/a	chr14:71787550-71787560 chr14:71787028-71787037 chr14:71787925-71787935
39	CHD2	chr14:71788124-71788374	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr14:71787751-71787753	K562	blood:	n/a	n/a
41	CHD2	chr14:71786620-71789089	Hela-S3	cervix:	n/a	chr14:71787550-71787560 chr14:71787028-71787037 chr14:71787925-71787935
42	CHD2	chr14:71786733-71787821	HepG2	liver:	n/a	chr14:71787550-71787560 chr14:71787028-71787037
43	CHD2	chr14:71786488-71788320	GM12878	blood:	n/a	chr14:71787550-71787560 chr14:71787028-71787037 chr14:71787925-71787935
44	CHD2	chr14:71786411-71787503	H1-hESC	embryonic stem cell:	n/a	chr14:71787028-71787037
45	CHD2	chr14:71786665-71787435	K562	blood:	n/a	chr14:71787028-71787037
46	CREB1	chr14:71786799-71787354	A549	lung:	n/a	n/a
47	CREB1	chr14:71786744-71787612	GM12878	blood:	n/a	n/a
48	CTBP2	chr14:71786751-71787915	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr14:71788115-71788961	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr14:71786860-71787010	AG04449	skin:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71787215-71787265	AG04449	skin:	fetal
2	chr14:71787215-71787265	AG04449	skin:	fetal
3	chr14:71787552-71787602	PANC-1	pancreas:	n/a
4	chr14:71788528-71788578	AoSMC	blood vessel:	n/a
5	chr14:71788121-71788171	HCF	heart:	n/a
6	chr14:71788121-71788171	HPAEpiC	pulmonary alveolar:	n/a
7	chr14:71786811-71786861	NT2-D1	testis:	n/a
8	chr14:71787215-71787265	NB4	blood:	n/a
9	chr14:71788528-71788578	Hela-S3	cervix:	n/a
10	chr14:71787570-71787620	HRPEpiC	eye:	n/a
11	chr14:71787570-71787620	HRCEpiC	kidney:	n/a
12	chr14:71787570-71787620	HCF	heart:	n/a
13	chr14:71787552-71787602	AG09319	gingival:	n/a
14	chr14:71788121-71788171	AG09319	gingival:	n/a
15	chr14:71787552-71787602	HNPCEpiC	eye:	n/a
16	chr14:71786811-71786861	GM12892	blood:	n/a
17	chr14:71787996-71788046	HCF	heart:	n/a
18	chr14:71788121-71788171	HepG2	liver:	n/a
19	chr14:71787215-71787265	K562	blood:	n/a
20	chr14:71788121-71788171	HCT-116	colon:	n/a
21	chr14:71788528-71788578	GM12878	blood:	n/a
22	chr14:71786911-71786961	SAEC	small airway:	n/a
23	chr14:71787552-71787602	HEK293	kidney:	embryo
24	chr14:71787570-71787620	ECC-1	luminal epithelium:	n/a
25	chr14:71786811-71786861	HCF	heart:	n/a
26	chr14:71787552-71787602	CMK	blood:	n/a
27	chr14:71788121-71788171	GM12878	blood:	n/a
28	chr14:71788121-71788171	SKMC	muscle:	n/a
29	chr14:71788528-71788578	SK-N-MC	brain:	n/a
30	chr14:71786911-71786961	Hepatocyte	liver:	n/a
31	chr14:71787552-71787602	U87	brain:	n/a
32	chr14:71786911-71786961	HNPCEpiC	eye:	n/a
33	chr14:71788528-71788578	GM12892	blood:	n/a
34	chr14:71786811-71786861	Hepatocyte	liver:	n/a
35	chr14:71788121-71788171	PANC-1	pancreas:	n/a
36	chr14:71787570-71787620	PFSK-1	brain:	n/a
37	chr14:71788528-71788578	HUVEC	blood vessel:	n/a
38	chr14:71787552-71787602	ProgFib	skin:	n/a
39	chr14:71787570-71787620	SKMC	muscle:	n/a
40	chr14:71788121-71788171	AG10803	skin:	n/a
41	chr14:71787552-71787602	AG09309	skin:	n/a
42	chr14:71787996-71788046	MCF10A-Er-Src	breast:	n/a
43	chr14:71787996-71788046	H1-hESC	embryonic stem cell:	embryo
44	chr14:71787996-71788046	AG09319	gingival:	n/a
45	chr14:71787552-71787602	SK-N-MC	brain:	n/a
46	chr14:71788528-71788578	AG04449	skin:	fetal
47	chr14:71787552-71787602	PrEC	prostate:	n/a
48	chr14:71787570-71787620	BJ	skin:	n/a
49	chr14:71787215-71787265	ProgFib	skin:	n/a
50	chr14:71787996-71788046	GM12878	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:71786623..71788661-chr14:71864889..71866852,2	MCF-7	breast:
2	chr14:71780085..71783168-chr14:71784973..71787067,3	K562	blood:
3	chr14:71787414..71788237-chr2:85766306..85767247,2	Hela-S3	cervix:
4	chr14:71608562..71610263-chr14:71786915..71789760,2	MCF-7	breast:
5	chr1:24127046..24127839-chr14:71786977..71787974,2	Hela-S3	cervix:
6	chr14:71647115..71649453-chr14:71786412..71788278,2	MCF-7	breast:
7	chr14:71776798..71778756-chr14:71785140..71789113,3	MCF-7	breast:
8	chr14:71787272..71789927-chr14:72149469..72152199,2	MCF-7	breast:
9	chr14:71786721..71787223-chr19:9929449..9930057,2	NB4	blood:
10	chr14:71787090..71788740-chr14:71796543..71798453,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP3K9-3	chr14:71786892-71787882	XLOC_011064
2	lnc-MAP3K9-3	chr14:71788391-71788653	XLOC_011064
3	lnc-MAP3K9-3	chr14:71788391-71788531	ENSG00000259146.1
4	lnc-MAP3K9-3	chr14:71786174-71786271	XLOC_011064
5	lnc-MAP3K9-3	chr14:71786174-71786298	NONHSAT037628
6	lnc-MAP3K9-3	chr14:71788391-71788532	XLOC_011064
7	lnc-MAP3K9-3	chr14:71786174-71786271	XLOC_011064
8	lnc-SIPA1L1-2	chr14:71787839-71787898	NONHSAT037631
9	lnc-SIPA1L1-2	chr14:71787190-71787220	NONHSAT037631
10	lnc-MAP3K9-3	chr14:71788499-71788530	XLOC_011064
11	lnc-MAP3K9-3	chr14:71786892-71787038	XLOC_011064

No data

Variant related genes	Relation type
ENSG00000259146	TF binding region
SIPA1L1	TF binding region
ENSG00000259146	CpG island
SIPA1L1	CpG island
ENSG00000127452	chromatin interactions
ENSG00000117308	chromatin interactions
ENSG00000259146	chromatin interactions
ENSG00000269927	chromatin interactions
ENSG00000197555	chromatin interactions
ENSG00000259079	chromatin interactions
ENSG00000207444	chromatin interactions
ENSG00000259907	chromatin interactions
ENSG00000168906	chromatin interactions
HELZ	miRNA target sites
AKAP12	miRNA target sites
CD46	miRNA target sites
RBM46	miRNA target sites

Extended variants
information (count: 95 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557781708	chr14:71786230-71786231	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs58026156	chr14:71786249-71786250	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs555998438	chr14:71786259-71786260	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs140269121	chr14:71786267-71786268	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs190984599	chr14:71786289-71786290	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs529225867	chr14:71786294-71786295	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs553642849	chr14:71786321-71786322	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572043646	chr14:71786347-71786348	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs75853744	chr14:71786366-71786367	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116150606	chr14:71786389-71786390	Flanking Active TSS Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs183076343	chr14:71786439-71786440	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs547717608	chr14:71786470-71786471	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs34635034	chr14:71786484-71786485	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs6574012	chr14:71786492-71786493	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs562971929	chr14:71786504-71786505	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs530112469	chr14:71786527-71786528	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs58376573	chr14:71786548-71786549	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560749808	chr14:71786562-71786563	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs55763740	chr14:71786563-71786564	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs187726013	chr14:71786584-71786585	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs191461980	chr14:71786602-71786603	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs538060660	chr14:71786633-71786634	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs577739877	chr14:71786644-71786645	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs549464864	chr14:71786745-71786746	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs145329845	chr14:71786786-71786787	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs202229852	chr14:71786849-71786850	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs535067742	chr14:71786866-71786867	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs553380873	chr14:71786913-71786914	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs571968814	chr14:71786947-71786948	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
30	rs539685833	chr14:71787023-71787024	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
31	rs557776720	chr14:71787029-71787030	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs576139750	chr14:71787044-71787045	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs543298493	chr14:71787128-71787129	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
34	rs556685151	chr14:71787170-71787171	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
35	rs575018229	chr14:71787172-71787173	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
36	rs182486690	chr14:71787187-71787188	Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
37	rs560482653	chr14:71787269-71787270	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs527697997	chr14:71787293-71787294	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
39	rs546432664	chr14:71787304-71787305	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
40	rs564676051	chr14:71787328-71787329	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
41	rs531925097	chr14:71787334-71787335	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
42	rs188390508	chr14:71787353-71787354	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
43	rs567795142	chr14:71787391-71787392	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
44	rs554670056	chr14:71787420-71787421	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
45	rs376923072	chr14:71787421-71787422	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
46	rs528927926	chr14:71787423-71787424	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
47	rs547106267	chr14:71787424-71787425	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
48	rs565629802	chr14:71787425-71787426	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
49	rs10129431	chr14:71787440-71787441	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs34093378	chr14:71787453-71787454	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71771800-71786400	Weak transcription	Pancreas	Pancrea
2	chr14:71779800-71786400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr14:71781800-71786400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:71781800-71786400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr14:71784400-71786400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr14:71784400-71786400	Weak transcription	Fetal Muscle Leg	muscle
7	chr14:71784600-71786400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:71784600-71786400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:71784600-71786400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr14:71784600-71786400	Weak transcription	Left Ventricle	heart
11	chr14:71784600-71786400	Weak transcription	Spleen	Spleen
12	chr14:71785000-71786400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr14:71786000-71786400	Enhancers	Dnd41	blood
14	chr14:71786000-71786600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr14:71786000-71789200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr14:71786200-71786400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr14:71786200-71786400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:71786200-71786400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:71786200-71786400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr14:71786200-71786400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:71786200-71786400	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr14:71786200-71786400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:71786200-71786400	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr14:71786200-71786400	Enhancers	Primary B cells from cord blood	blood
25	chr14:71786200-71786400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr14:71786200-71786400	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr14:71786200-71786400	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr14:71786200-71786400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr14:71786200-71786400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:71786200-71786400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:71786200-71786400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr14:71786200-71786400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:71786200-71786400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:71786200-71786400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:71786200-71786400	Enhancers	Adipose Nuclei	Adipose
36	chr14:71786200-71786400	Enhancers	Brain Anterior Caudate	brain
37	chr14:71786200-71786400	Enhancers	Brain Cingulate Gyrus	brain
38	chr14:71786200-71786400	Enhancers	Brain Germinal Matrix	brain
39	chr14:71786200-71786400	Enhancers	Brain Substantia Nigra	brain
40	chr14:71786200-71786400	Enhancers	Colon Smooth Muscle	Colon
41	chr14:71786200-71786400	Enhancers	Fetal Intestine Large	intestine
42	chr14:71786200-71786400	Enhancers	Fetal Intestine Small	intestine
43	chr14:71786200-71786400	Enhancers	Fetal Kidney	kidney
44	chr14:71786200-71786400	Enhancers	Psoas Muscle	Psoas
45	chr14:71786200-71786400	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr14:71786200-71786400	Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr14:71786200-71786400	Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr14:71786200-71786400	Enhancers	Thymus	Thymus
49	chr14:71786200-71786400	Enhancers	HepG2	liver
50	chr14:71786200-71786400	Active TSS	HMEC	breast

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