Variant report

Variant	nsv85164
Chromosome Location	chr14:97207464-97209699
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	BACH1	chr14:97207734-97208439	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr14:97207870-97208044	K562	blood:	n/a	chr14:97208000-97208016
3	BHLHE40	chr14:97207789-97208039	GM12878	blood:	n/a	chr14:97208000-97208016
4	CBX3	chr14:97207726-97208048	K562	blood:	n/a	n/a
5	CEBPB	chr14:97207775-97208037	Hela-S3	cervix:	n/a	n/a
6	CHD1	chr14:97207865-97207996	GM12878	blood:	n/a	n/a
7	CHD2	chr14:97207819-97207959	GM12878	blood:	n/a	n/a
8	CHD2	chr14:97207903-97208007	Hela-S3	cervix:	n/a	n/a
9	CREB1	chr14:97207741-97208070	A549	lung:	n/a	n/a
10	CREB1	chr14:97207775-97207987	A549	lung:	n/a	n/a
11	CREB1	chr14:97207698-97208064	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr14:97207739-97208019	A549	lung:	n/a	chr14:97207934-97207950
13	CTCF	chr14:97207820-97207970	GM12874	blood:	n/a	chr14:97207934-97207950
14	CTCF	chr14:97208540-97208690	GM12870	blood:	n/a	n/a
15	CTCF	chr14:97207840-97207990	GM12869	blood:	n/a	chr14:97207934-97207950
16	CTCF	chr14:97207397-97208189	A549	lung:	n/a	chr14:97207934-97207950 chr14:97208174-97208184 chr14:97208173-97208186
17	CTCF	chr14:97207789-97208065	Lung_OC	lung:	n/a	chr14:97207934-97207950
18	CTCF	chr14:97207800-97208026	SK-N-SH_RA	brain:	n/a	chr14:97207934-97207950
19	CTCF	chr14:97207689-97208072	HCT-116	colon:	n/a	chr14:97207934-97207950
20	CTCF	chr14:97207772-97208112	A549	lung:	n/a	chr14:97207934-97207950
21	CTCF	chr14:97207860-97208010	GM12870	blood:	n/a	chr14:97207934-97207950
22	CTCF	chr14:97207776-97208096	MCF-7	breast:	n/a	chr14:97207934-97207950
23	CTCF	chr14:97207810-97208076	Pancreas_OC	pancreas:	n/a	chr14:97207934-97207950
24	CTCF	chr14:97207860-97208010	NHEK	skin:	n/a	chr14:97207934-97207950
25	CTCF	chr14:97207860-97208010	HEK293	kidney:	n/a	chr14:97207934-97207950
26	CTCF	chr14:97207840-97207990	MCF-7	breast:	n/a	chr14:97207934-97207950
27	CTCF	chr14:97207840-97207990	HCT-116	colon:	n/a	chr14:97207934-97207950
28	CTCF	chr14:97207816-97208071	Kidney_OC	kidney:	n/a	chr14:97207934-97207950
29	CTCF	chr14:97207880-97208030	HMF	breast:	n/a	chr14:97207934-97207950
30	CTCF	chr14:97207880-97208030	NB4	blood:	n/a	chr14:97207934-97207950
31	CTCF	chr14:97207860-97208010	HRE	kidney:	n/a	chr14:97207934-97207950
32	CTCF	chr14:97207705-97208133	H1-hESC	embryonic stem cell:	n/a	chr14:97207934-97207950
33	CTCF	chr14:97207500-97207650	GM12875	blood:	n/a	n/a
34	CTCF	chr14:97207762-97208073	K562	blood:	n/a	chr14:97207934-97207950
35	CTCF	chr14:97207860-97208010	GM12875	blood:	n/a	chr14:97207934-97207950
36	CTCF	chr14:97207840-97207990	A549	lung:	n/a	chr14:97207934-97207950
37	CTCF	chr14:97207825-97208006	HUVEC	blood vessel:	n/a	chr14:97207934-97207950
38	CTCF	chr14:97207860-97208010	K562	blood:	n/a	chr14:97207934-97207950
39	CTCF	chr14:97207784-97208082	Fibrobl	skin:	n/a	chr14:97207934-97207950
40	CTCF	chr14:97207840-97207990	AG04450	lung:	n/a	chr14:97207934-97207950
41	CTCF	chr14:97207773-97208078	MCF-7	breast:	n/a	chr14:97207934-97207950
42	CTCF	chr14:97207796-97208074	Medullo	brain:	n/a	chr14:97207934-97207950
43	CTCF	chr14:97207860-97208010	HRPEpiC	eye:	n/a	chr14:97207934-97207950
44	CTCF	chr14:97207860-97208010	HCPEpiC	choroid plexus:	n/a	chr14:97207934-97207950
45	CTCF	chr14:97208120-97208270	HCPEpiC	choroid plexus:	n/a	chr14:97208174-97208184 chr14:97208173-97208186
46	CTCF	chr14:97207671-97208212	MCF-7	breast:	n/a	chr14:97207934-97207950 chr14:97208174-97208184 chr14:97208173-97208186
47	CTCF	chr14:97207860-97208010	GM12865	blood:	n/a	chr14:97207934-97207950
48	CTCF	chr14:97207791-97208082	GM10248	blood:	n/a	chr14:97207934-97207950
49	CTCF	chr14:97207775-97208086	NHEK	skin:	n/a	chr14:97207934-97207950
50	CTCF	chr14:97207860-97208010	HepG2	liver:	n/a	chr14:97207934-97207950

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97208245-97208295	HRCEpiC	kidney:	n/a
2	chr14:97208245-97208295	HRCEpiC	kidney:	n/a
3	chr14:97208170-97208220	HCT-116	colon:	n/a
4	chr14:97208170-97208220	HCM	heart:	n/a
5	chr14:97209298-97209348	HCT-116	colon:	n/a
6	chr14:97207786-97207836	HRPEpiC	eye:	n/a
7	chr14:97209298-97209348	Jurkat	blood:	n/a
8	chr14:97208245-97208295	HIPEpiC	eye:	n/a
9	chr14:97208170-97208220	ovcar-3	ovarian:	n/a
10	chr14:97208114-97208164	SK-N-SH	brain:	n/a
11	chr14:97208245-97208295	SKMC	muscle:	n/a
12	chr14:97208245-97208295	HUVEC	blood vessel:	n/a
13	chr14:97208333-97208383	GM19239	blood:	n/a
14	chr14:97209298-97209348	RPTEC	kidney:	n/a
15	chr14:97209298-97209348	ovcar-3	ovarian:	n/a
16	chr14:97208114-97208164	PrEC	prostate:	n/a
17	chr14:97208333-97208383	MCF-7	breast:	n/a
18	chr14:97209298-97209348	NH-A	brain:	n/a
19	chr14:97208114-97208164	SK-N-MC	brain:	n/a
20	chr14:97209298-97209348	HIPEpiC	eye:	n/a
21	chr14:97208114-97208164	Caco-2	colon:	n/a
22	chr14:97208114-97208164	SK-N-SH_RA	brain:	n/a
23	chr14:97208333-97208383	GM12891	blood:	n/a
24	chr14:97209298-97209348	NHDF-neo	bronchial:	n/a
25	chr14:97208170-97208220	HRPEpiC	eye:	n/a
26	chr14:97207786-97207836	RPTEC	kidney:	n/a
27	chr14:97207786-97207836	NT2-D1	testis:	n/a
28	chr14:97208245-97208295	AG10803	skin:	n/a
29	chr14:97208114-97208164	NT2-D1	testis:	n/a
30	chr14:97208170-97208220	HEEpiC	esophagus:	n/a
31	chr14:97208333-97208383	HRCEpiC	kidney:	n/a
32	chr14:97209298-97209348	BJ	skin:	n/a
33	chr14:97209298-97209348	Hela-S3	cervix:	n/a
34	chr14:97208333-97208383	AG09319	gingival:	n/a
35	chr14:97208245-97208295	SK-N-SH	brain:	n/a
36	chr14:97208333-97208383	SKMC	muscle:	n/a
37	chr14:97209298-97209348	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:97208333-97208383	A549	lung:	n/a
39	chr14:97208114-97208164	HCF	heart:	n/a
40	chr14:97208170-97208220	U87	brain:	n/a
41	chr14:97208170-97208220	MCF10A-Er-Src	breast:	n/a
42	chr14:97207786-97207836	Caco-2	colon:	n/a
43	chr14:97208114-97208164	AG04449	skin:	fetal
44	chr14:97208333-97208383	ovcar-3	ovarian:	n/a
45	chr14:97208245-97208295	BE2_C	brain:	n/a
46	chr14:97208245-97208295	CMK	blood:	n/a
47	chr14:97207786-97207836	MCF10A-Er-Src	breast:	n/a
48	chr14:97208333-97208383	HNPCEpiC	eye:	n/a
49	chr14:97208245-97208295	GM19239	blood:	n/a
50	chr14:97208114-97208164	A549	lung:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK1-2	chr14:97207528-97207548	ENSG00000258979
2	lnc-ATG2B-9	chr14:97209419-97209532	ucscGeneNc_uc001yfv_1

Variant related genes	Relation type
ENSG00000258979	TF binding region
ENSG00000258979	CpG island

Extended variants
information (count: 86 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2025355	chr14:97207464-97207465	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs150111802	chr14:97207467-97207468	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143704070	chr14:97207470-97207471	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs8009078	chr14:97207473-97207474	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554611396	chr14:97207501-97207502	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs573379786	chr14:97207543-97207544	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
7	rs540774136	chr14:97207590-97207591	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs558411539	chr14:97207591-97207592	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs565450506	chr14:97207598-97207599	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs532882433	chr14:97207668-97207669	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78823311	chr14:97207676-97207677	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544898520	chr14:97207699-97207700	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs4284568	chr14:97207772-97207773	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562500263	chr14:97207779-97207780	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529678759	chr14:97207816-97207817	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs548326034	chr14:97207827-97207828	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs35467594	chr14:97207868-97207869	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs372903036	chr14:97207891-97207892	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs11623288	chr14:97207994-97207995	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs527500326	chr14:97208027-97208028	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs552387398	chr14:97208072-97208073	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs184832095	chr14:97208078-97208079	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs11160361	chr14:97208095-97208096	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs10146854	chr14:97208145-97208146	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568929082	chr14:97208191-97208192	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs113033521	chr14:97208198-97208199	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs554647863	chr14:97208232-97208233	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189436776	chr14:97208241-97208242	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376017560	chr14:97208285-97208286	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61979849	chr14:97208301-97208302	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs185767266	chr14:97208368-97208369	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75666069	chr14:97208381-97208382	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563146633	chr14:97208422-97208423	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543159031	chr14:97208449-97208450	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541803019	chr14:97208488-97208489	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561837296	chr14:97208508-97208509	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371959348	chr14:97208510-97208511	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542324633	chr14:97208534-97208535	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs71415050	chr14:97208549-97208550	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs113242072	chr14:97208558-97208559	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147181923	chr14:97208560-97208561	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527425275	chr14:97208564-97208565	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551966729	chr14:97208593-97208594	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564342556	chr14:97208594-97208595	Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373657669	chr14:97208607-97208608	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs531373184	chr14:97208613-97208614	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs368406628	chr14:97208657-97208658	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs369902687	chr14:97208692-97208693	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs59567559	chr14:97208717-97208718	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs536256559	chr14:97208764-97208765	Weak transcription Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97203400-97207600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:97206200-97208800	Enhancers	Fetal Brain Male	brain
3	chr14:97206400-97207600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:97206800-97208400	Bivalent/Poised TSS	HSMM	muscle
5	chr14:97207000-97207800	Flanking Active TSS	Fetal Brain Female	brain
6	chr14:97207200-97207600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:97207200-97207600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
8	chr14:97207200-97207600	Bivalent Enhancer	Brain Hippocampus Middle	brain
9	chr14:97207400-97207600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
10	chr14:97207400-97207600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:97207400-97207600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:97207400-97207600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:97207400-97207600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr14:97207400-97207600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr14:97207400-97207600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
16	chr14:97207400-97207600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
17	chr14:97207400-97207600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
18	chr14:97207400-97207600	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr14:97207400-97207600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
20	chr14:97207400-97207600	Bivalent Enhancer	Adipose Nuclei	Adipose
21	chr14:97207400-97207600	Enhancers	Liver	Liver
22	chr14:97207400-97207600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
23	chr14:97207400-97207600	Flanking Active TSS	Brain Substantia Nigra	brain
24	chr14:97207400-97207600	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
25	chr14:97207400-97207600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
26	chr14:97207400-97207600	Bivalent Enhancer	Fetal Intestine Large	intestine
27	chr14:97207400-97207600	Bivalent Enhancer	Fetal Intestine Small	intestine
28	chr14:97207400-97207600	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr14:97207400-97207600	Bivalent Enhancer	Fetal Thymus	thymus
30	chr14:97207400-97207600	Bivalent Enhancer	Rectal Smooth Muscle	rectum
31	chr14:97207400-97207600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr14:97207400-97207600	Bivalent Enhancer	Dnd41	blood
33	chr14:97207400-97207600	Bivalent Enhancer	HMEC	breast
34	chr14:97207400-97207600	Bivalent/Poised TSS	NHDF-Ad	bronchial
35	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:97207400-97207800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
38	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
40	chr14:97207400-97207800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
41	chr14:97207400-97207800	Bivalent/Poised TSS	Primary T helper naive cells from peripheral blood	blood
42	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
43	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:97207400-97207800	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
45	chr14:97207400-97207800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr14:97207400-97207800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr14:97207400-97207800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:97207400-97207800	Flanking Active TSS	Brain Germinal Matrix	brain
49	chr14:97207400-97207800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr14:97207400-97207800	Bivalent Enhancer	Fetal Heart	heart

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