Variant report

Variant	nsv565005
Chromosome Location	chr14:70039587-70040957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr14:70040900-70041050	HCM	heart:	n/a	n/a
2	E2F6	chr14:70038151-70039756	A549	lung:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70038869-70038880 chr14:70039085-70039095
3	E2F6	chr14:70037838-70041874	H1-hESC	embryonic stem cell:	n/a	chr14:70039917-70039926 chr14:70040055-70040065 chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70039907-70039917 chr14:70038869-70038880 chr14:70041273-70041288 chr14:70041340-70041349 chr14:70039085-70039095
4	E2F6	chr14:70038047-70039768	H1-hESC	embryonic stem cell:	n/a	chr14:70039052-70039062 chr14:70039095-70039104 chr14:70039088-70039098 chr14:70038869-70038880 chr14:70039085-70039095
5	GABPA	chr14:70039041-70039653	H1-hESC	embryonic stem cell:	n/a	n/a
6	GABPA	chr14:70040363-70040890	H1-hESC	embryonic stem cell:	n/a	n/a
7	GTF2F1	chr14:70040637-70040762	H1-hESC	embryonic stem cell:	n/a	n/a
8	MAX	chr14:70038011-70039766	ECC-1	luminal epithelium:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70039728-70039737 chr14:70038304-70038313 chr14:70038305-70038312
9	MAX	chr14:70038055-70039799	H1-hESC	embryonic stem cell:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70039728-70039737 chr14:70038304-70038313 chr14:70038305-70038312
10	MAX	chr14:70039860-70040367	HepG2	liver:	n/a	n/a
11	MAX	chr14:70038054-70039747	ECC-1	luminal epithelium:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70039728-70039737 chr14:70038304-70038313 chr14:70038305-70038312
12	MAX	chr14:70038034-70039730	H1-hESC	embryonic stem cell:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70038304-70038313 chr14:70038305-70038312
13	MAX	chr14:70038147-70039969	A549	lung:	n/a	chr14:70038494-70038503 chr14:70039385-70039392 chr14:70039384-70039393 chr14:70039728-70039737 chr14:70038304-70038313 chr14:70038305-70038312
14	NFIC	chr14:70038434-70039623	ECC-1	luminal epithelium:	n/a	n/a
15	NFIC	chr14:70038297-70039637	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr14:70040474-70041009	H1-neurons	neurons:	n/a	n/a
17	POLR2A	chr14:70040391-70041771	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr14:70040539-70040540	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr14:70040949-70040975	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr14:70040554-70040945	H1-hESC	embryonic stem cell:	n/a	n/a
21	RAD21	chr14:70040860-70041982	SK-N-SH	brain:	n/a	chr14:70041603-70041616 chr14:70041312-70041322 chr14:70041602-70041614 chr14:70041140-70041153 chr14:70041604-70041614
22	REST	chr14:70040120-70042029	H1-neurons	neurons:	n/a	chr14:70041308-70041317 chr14:70040123-70040141 chr14:70040122-70040142 chr14:70040518-70040531 chr14:70040126-70040139 chr14:70040129-70040142 chr14:70040122-70040142
23	TAF1	chr14:70040847-70041701	H1-neurons	neurons:	n/a	n/a
24	TCF12	chr14:70038272-70039602	ECC-1	luminal epithelium:	n/a	chr14:70038848-70038858 chr14:70038849-70038856
25	TCF12	chr14:70040533-70040851	H1-hESC	embryonic stem cell:	n/a	n/a
26	TCF12	chr14:70040545-70040792	H1-hESC	embryonic stem cell:	n/a	n/a
27	TCF7L2	chr14:70040492-70040910	HEK293	kidney:	n/a	n/a
28	TEAD4	chr14:70040352-70040891	H1-hESC	embryonic stem cell:	n/a	n/a
29	TEAD4	chr14:70040461-70040858	H1-hESC	embryonic stem cell:	n/a	n/a
30	ZNF263	chr14:70040244-70040961	HEK293-T-REx	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70040391-70040441	ovcar-3	ovarian:	n/a
2	chr14:70040391-70040441	ovcar-3	ovarian:	n/a
3	chr14:70040899-70040949	PFSK-1	brain:	n/a
4	chr14:70039915-70039965	HL-60	blood:	n/a
5	chr14:70040899-70040949	Jurkat	blood:	n/a
6	chr14:70040899-70040949	NH-A	brain:	n/a
7	chr14:70039915-70039965	Hela-S3	cervix:	n/a
8	chr14:70040391-70040441	HPAEpiC	pulmonary alveolar:	n/a
9	chr14:70040899-70040949	GM19239	blood:	n/a
10	chr14:70040391-70040441	HRPEpiC	eye:	n/a
11	chr14:70040391-70040441	BE2_C	brain:	n/a
12	chr14:70040391-70040441	MCF10A-Er-Src	breast:	n/a
13	chr14:70040899-70040949	GM12892	blood:	n/a
14	chr14:70039915-70039965	HRCEpiC	kidney:	n/a
15	chr14:70040391-70040441	HRE	kidney:	n/a
16	chr14:70040899-70040949	A549	lung:	n/a
17	chr14:70039915-70039965	GM06990	blood:	n/a
18	chr14:70040899-70040949	T-47D	breast:	n/a
19	chr14:70040391-70040441	HNPCEpiC	eye:	n/a
20	chr14:70039915-70039965	NHBE	bronchial:	n/a
21	chr14:70039915-70039965	HNPCEpiC	eye:	n/a
22	chr14:70040391-70040441	HCPEpiC	choroid plexus:	n/a
23	chr14:70040899-70040949	SAEC	small airway:	n/a
24	chr14:70039915-70039965	H1-hESC	embryonic stem cell:	embryo
25	chr14:70039915-70039965	SAEC	small airway:	n/a
26	chr14:70039915-70039965	ECC-1	luminal epithelium:	n/a
27	chr14:70040391-70040441	NHBE	bronchial:	n/a
28	chr14:70039915-70039965	K562	blood:	n/a
29	chr14:70040391-70040441	HAEpiC	amniotic membrane:	n/a
30	chr14:70040899-70040949	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:70040391-70040441	MCF-7	breast:	n/a
32	chr14:70040899-70040949	HL-60	blood:	n/a
33	chr14:70039915-70039965	Hepatocyte	liver:	n/a
34	chr14:70039915-70039965	HEK293	kidney:	embryo
35	chr14:70039915-70039965	Caco-2	colon:	n/a
36	chr14:70039915-70039965	HCF	heart:	n/a
37	chr14:70040391-70040441	GM12878	blood:	n/a
38	chr14:70040391-70040441	GM12892	blood:	n/a
39	chr14:70040391-70040441	GM12891	blood:	n/a
40	chr14:70040899-70040949	HNPCEpiC	eye:	n/a
41	chr14:70040899-70040949	AG04450	lung:	fetal
42	chr14:70040391-70040441	SK-N-MC	brain:	n/a
43	chr14:70039915-70039965	GM12878	blood:	n/a
44	chr14:70040899-70040949	CMK	blood:	n/a
45	chr14:70040391-70040441	GM06990	blood:	n/a
46	chr14:70039915-70039965	SKMC	muscle:	n/a
47	chr14:70039915-70039965	SK-N-SH_RA	brain:	n/a
48	chr14:70040899-70040949	HCT-116	colon:	n/a
49	chr14:70040391-70040441	HCF	heart:	n/a
50	chr14:70040899-70040949	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:69949714..69952374-chr14:70039182..70041131,3	MCF-7	breast:
2	chr14:70036912..70038706-chr14:70040330..70041890,2	MCF-7	breast:
3	chr14:70037278..70041103-chr14:70232570..70234461,4	MCF-7	breast:
4	chr14:70001699..70002644-chr14:70040741..70042019,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000267909	TF binding region
CCDC177	TF binding region
ENSG00000267909	CpG island
CCDC177	CpG island
ENSG00000255994	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000175985	chromatin interactions

Extended variants
information (count: 44 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7147881	chr14:70039587-70039588	ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554873304	chr14:70039662-70039663	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs554539552	chr14:70039672-70039673	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs540146735	chr14:70039694-70039695	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs202100921	chr14:70039803-70039804	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs375620132	chr14:70039804-70039805	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs60812300	chr14:70039809-70039810	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4048622	chr14:70039824-70039825	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs4902734	chr14:70039881-70039882	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540885499	chr14:70039916-70039917	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs559226383	chr14:70040019-70040020	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs6573892	chr14:70040223-70040224	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544861271	chr14:70040227-70040228	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs563526840	chr14:70040241-70040242	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs530519555	chr14:70040255-70040256	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs117298196	chr14:70040280-70040281	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs576968208	chr14:70040291-70040292	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190804679	chr14:70040293-70040294	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528099391	chr14:70040313-70040314	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs138905072	chr14:70040359-70040360	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs558596005	chr14:70040378-70040379	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs113077435	chr14:70040391-70040392	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs183327144	chr14:70040407-70040408	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs539351154	chr14:70040411-70040412	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs540809779	chr14:70040425-70040426	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs550871201	chr14:70040429-70040430	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs569479375	chr14:70040432-70040433	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs560787174	chr14:70040442-70040443	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs554652060	chr14:70040461-70040462	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs572854793	chr14:70040489-70040490	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs35211808	chr14:70040542-70040543	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs533953547	chr14:70040547-70040548	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs558562910	chr14:70040558-70040559	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs367774228	chr14:70040579-70040580	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs74061860	chr14:70040637-70040638	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs74061861	chr14:70040638-70040639	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs575407890	chr14:70040672-70040673	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs542700336	chr14:70040702-70040703	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs551156457	chr14:70040738-70040739	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs560989757	chr14:70040784-70040785	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs528054941	chr14:70040820-70040821	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs544176750	chr14:70040859-70040860	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs574391372	chr14:70040872-70040873	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs546601300	chr14:70040926-70040927	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	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	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	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

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70036600-70039600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:70036600-70040200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:70037200-70039600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:70037400-70039600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:70037400-70040200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr14:70037600-70039600	Bivalent Enhancer	Placenta	Placenta
7	chr14:70037800-70039600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:70037800-70040200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:70037800-70040400	Enhancers	Fetal Brain Male	brain
10	chr14:70038000-70039600	Bivalent Enhancer	Fetal Heart	heart
11	chr14:70038000-70040400	Enhancers	Liver	Liver
12	chr14:70038000-70040400	Weak transcription	Brain Angular Gyrus	brain
13	chr14:70038000-70040400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr14:70038000-70040400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr14:70038200-70039600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
16	chr14:70038200-70039600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:70038200-70039600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:70038200-70039600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr14:70038200-70039600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
20	chr14:70038200-70040600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
21	chr14:70038200-70040600	Bivalent Enhancer	Stomach Mucosa	stomach
22	chr14:70038200-70040800	Flanking Bivalent TSS/Enh	Right Ventricle	heart
23	chr14:70038200-70040800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
24	chr14:70038400-70039600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr14:70038400-70039600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:70038400-70039600	ZNF genes & repeats	Brain Germinal Matrix	brain
27	chr14:70038400-70039600	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
28	chr14:70038400-70039600	Flanking Active TSS	Right Atrium	heart
29	chr14:70038400-70039800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
30	chr14:70038400-70039800	Strong transcription	Fetal Brain Female	brain
31	chr14:70038400-70040000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr14:70038400-70040800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:70038600-70039600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr14:70038600-70039600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
35	chr14:70038600-70039600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
36	chr14:70038600-70039600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr14:70038600-70039600	Bivalent/Poised TSS	A549	lung
38	chr14:70038600-70040000	Bivalent/Poised TSS	HSMM	muscle
39	chr14:70038600-70040200	Bivalent/Poised TSS	HepG2	liver
40	chr14:70038800-70039600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
41	chr14:70038800-70039600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr14:70038800-70039600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
43	chr14:70039000-70039600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
44	chr14:70039000-70039600	Flanking Bivalent TSS/Enh	Left Ventricle	heart
45	chr14:70039000-70039600	Flanking Bivalent TSS/Enh	Ovary	ovary
46	chr14:70039000-70040000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:70039000-70041400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
48	chr14:70039200-70039600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:70039200-70039600	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr14:70039200-70039600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose

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