Variant report

Variant	esv3443202
Chromosome Location	chr8:65492948-65495196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:65493700-65494352	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:65492277-65493010	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:65494440-65494708	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:65494421-65494786	MCF-7	breast:	n/a	n/a
5	CHD1	chr8:65493406-65493604	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr8:65494053-65494609	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD1	chr8:65491785-65495139	GM12878	blood:	n/a	chr8:65492726-65492733
8	CHD2	chr8:65492149-65493115	GM12878	blood:	n/a	chr8:65492726-65492733
9	CHD2	chr8:65494069-65494262	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr8:65493408-65493757	GM12878	blood:	n/a	n/a
11	CHD2	chr8:65494356-65494927	GM12878	blood:	n/a	n/a
12	CHD2	chr8:65493985-65494085	GM12878	blood:	n/a	n/a
13	CTBP2	chr8:65492814-65494720	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:65494542-65494699	GM12878	blood:	n/a	n/a
15	CTCF	chr8:65493440-65493620	GM19238	blood:	n/a	n/a
16	CTCF	chr8:65493465-65493581	GM12891	blood:	n/a	n/a
17	CTCF	chr8:65493440-65493590	GM12864	blood:	n/a	n/a
18	CTCF	chr8:65493398-65493753	GM12878	blood:	n/a	n/a
19	CTCF	chr8:65493440-65493590	GM12874	blood:	n/a	n/a
20	CTCF	chr8:65494101-65494318	GM12892	blood:	n/a	n/a
21	CTCF	chr8:65493500-65493650	GM12866	blood:	n/a	n/a
22	CTCF	chr8:65493400-65493550	GM12871	blood:	n/a	n/a
23	CTCF	chr8:65493541-65493557	GM19240	blood:	n/a	n/a
24	CTCF	chr8:65493420-65493570	GM12872	blood:	n/a	n/a
25	CTCF	chr8:65493460-65493610	GM12874	blood:	n/a	n/a
26	CTCF	chr8:65493674-65493704	GM10266	blood:	n/a	n/a
27	CTCF	chr8:65494146-65494210	GM19238	blood:	n/a	n/a
28	CTCF	chr8:65493460-65493610	GM12878	blood:	n/a	n/a
29	CTCF	chr8:65493320-65493470	GM12871	blood:	n/a	n/a
30	CTCF	chr8:65493460-65493610	GM12868	blood:	n/a	n/a
31	CTCF	chr8:65493489-65493588	GM19239	blood:	n/a	n/a
32	CTCF	chr8:65494000-65494150	GM12867	blood:	n/a	n/a
33	CTCF	chr8:65493540-65493690	GM12869	blood:	n/a	n/a
34	CTCF	chr8:65493450-65493611	GM12892	blood:	n/a	n/a
35	CTCF	chr8:65493440-65493590	GM06990	blood:	n/a	n/a
36	CTCF	chr8:65493492-65493622	GM10248	blood:	n/a	n/a
37	CTCF	chr8:65493560-65493710	GM12873	blood:	n/a	n/a
38	CTCF	chr8:65494128-65494229	GM19239	blood:	n/a	n/a
39	CTCF	chr8:65493440-65493590	GM12867	blood:	n/a	n/a
40	CTCF	chr8:65493440-65493590	HEK293	kidney:	n/a	n/a
41	CTCF	chr8:65493680-65493830	GM12872	blood:	n/a	n/a
42	CTCF	chr8:65494200-65494350	GM12869	blood:	n/a	n/a
43	CTCF	chr8:65493440-65493590	GM12865	blood:	n/a	n/a
44	CTCF	chr8:65494120-65494290	GM12891	blood:	n/a	n/a
45	CTCF	chr8:65492747-65493031	GM12878	blood:	n/a	n/a
46	CTCF	chr8:65493360-65493510	GM12875	blood:	n/a	n/a
47	CTCF	chr8:65494160-65494310	GM12869	blood:	n/a	n/a
48	CTCF	chr8:65494266-65494279	GM12878	blood:	n/a	n/a
49	CUX1	chr8:65492624-65492952	GM12878	blood:	n/a	n/a
50	E2F6	chr8:65493307-65494323	H1-hESC	embryonic stem cell:	n/a	chr8:65493332-65493341 chr8:65493334-65493343

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:65493706-65493756	PrEC	prostate:	n/a
2	chr8:65493706-65493756	T-47D	breast:	n/a
3	chr8:65494451-65494501	HNPCEpiC	eye:	n/a
4	chr8:65494101-65494151	BE2_C	brain:	n/a
5	chr8:65492936-65492986	HPAEpiC	pulmonary alveolar:	n/a
6	chr8:65493706-65493756	IMR90	lung:	fetal
7	chr8:65494101-65494151	SK-N-MC	brain:	n/a
8	chr8:65494451-65494501	PANC-1	pancreas:	n/a
9	chr8:65494101-65494151	GM06990	blood:	n/a
10	chr8:65494101-65494151	HIPEpiC	eye:	n/a
11	chr8:65493706-65493756	PANC-1	pancreas:	n/a
12	chr8:65492936-65492986	HCT-116	colon:	n/a
13	chr8:65492936-65492986	HCM	heart:	n/a
14	chr8:65493706-65493756	SAEC	small airway:	n/a
15	chr8:65493706-65493756	PFSK-1	brain:	n/a
16	chr8:65493706-65493756	HRCEpiC	kidney:	n/a
17	chr8:65494785-65494835	HUVEC	blood vessel:	n/a
18	chr8:65493706-65493756	ovcar-3	ovarian:	n/a
19	chr8:65494785-65494835	H1-hESC	embryonic stem cell:	embryo
20	chr8:65494101-65494151	NHBE	bronchial:	n/a
21	chr8:65494785-65494835	BE2_C	brain:	n/a
22	chr8:65494101-65494151	HCPEpiC	choroid plexus:	n/a
23	chr8:65494451-65494501	PrEC	prostate:	n/a
24	chr8:65493706-65493756	HUVEC	blood vessel:	n/a
25	chr8:65494785-65494835	AG04450	lung:	fetal
26	chr8:65493706-65493756	A549	lung:	n/a
27	chr8:65492936-65492986	PANC-1	pancreas:	n/a
28	chr8:65494451-65494501	HCPEpiC	choroid plexus:	n/a
29	chr8:65494101-65494151	PFSK-1	brain:	n/a
30	chr8:65494785-65494835	CMK	blood:	n/a
31	chr8:65494785-65494835	SAEC	small airway:	n/a
32	chr8:65494451-65494501	NHDF-neo	bronchial:	n/a
33	chr8:65494101-65494151	GM12878	blood:	n/a
34	chr8:65494101-65494151	SK-N-SH	brain:	n/a
35	chr8:65492936-65492986	NB4	blood:	n/a
36	chr8:65493706-65493756	AG04449	skin:	fetal
37	chr8:65492936-65492986	RPTEC	kidney:	n/a
38	chr8:65494785-65494835	HIPEpiC	eye:	n/a
39	chr8:65492936-65492986	A549	lung:	n/a
40	chr8:65494785-65494835	HCT-116	colon:	n/a
41	chr8:65493706-65493756	BE2_C	brain:	n/a
42	chr8:65493706-65493756	HCT-116	colon:	n/a
43	chr8:65494451-65494501	MCF-7	breast:	n/a
44	chr8:65494785-65494835	Jurkat	blood:	n/a
45	chr8:65494785-65494835	LNCaP	prostate:	n/a
46	chr8:65494101-65494151	HPAEpiC	pulmonary alveolar:	n/a
47	chr8:65494785-65494835	Hela-S3	cervix:	n/a
48	chr8:65494785-65494835	SKMC	muscle:	n/a
49	chr8:65493706-65493756	HAEpiC	amniotic membrane:	n/a
50	chr8:65492936-65492986	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
ENSG00000254102	TF binding region
ENSG00000254102	CpG island

Extended variants
information (count: 101 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570829014	chr8:65492949-65492950	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs535029447	chr8:65493025-65493026	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs35739870	chr8:65493033-65493034	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs578248465	chr8:65493035-65493036	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs547029640	chr8:65493037-65493038	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs568463478	chr8:65493050-65493051	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs535635282	chr8:65493071-65493072	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556916817	chr8:65493084-65493085	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs575177094	chr8:65493166-65493167	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs539378603	chr8:65493172-65493173	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs557653288	chr8:65493287-65493288	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs34256577	chr8:65493291-65493292	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs35315475	chr8:65493293-65493294	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs572474539	chr8:65493326-65493327	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs539859044	chr8:65493378-65493379	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs7016250	chr8:65493429-65493430	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs573703828	chr8:65493467-65493468	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs369575054	chr8:65493496-65493497	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs200609947	chr8:65493509-65493510	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs62519835	chr8:65493532-65493533	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531148752	chr8:65493548-65493549	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs552866928	chr8:65493584-65493585	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545764928	chr8:65493593-65493594	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs535310107	chr8:65493609-65493610	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544639534	chr8:65493617-65493618	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564778972	chr8:65493627-65493628	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs79173338	chr8:65493637-65493638	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs34461543	chr8:65493644-65493645	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs35033801	chr8:65493646-65493647	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528446663	chr8:65493649-65493650	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs13279074	chr8:65493664-65493665	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs568531922	chr8:65493674-65493675	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs35814011	chr8:65493688-65493689	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs34856132	chr8:65493693-65493694	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs199899043	chr8:65493758-65493759	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs34872817	chr8:65493847-65493848	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs550729373	chr8:65493933-65493934	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs568684347	chr8:65493947-65493948	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs539265530	chr8:65493964-65493965	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs557592166	chr8:65493967-65493968	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs572806022	chr8:65493976-65493977	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs191620115	chr8:65494007-65494008	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564889045	chr8:65494020-65494021	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs34265378	chr8:65494021-65494022	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs62519837	chr8:65494023-65494024	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs62519838	chr8:65494026-65494027	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs71561231	chr8:65494048-65494049	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533783668	chr8:65494070-65494071	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs372721285	chr8:65494079-65494080	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs140123212	chr8:65494148-65494149	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Autism	20531469	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:65490800-65495000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
2	chr8:65491600-65493000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
3	chr8:65491600-65494400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
4	chr8:65491800-65493000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
5	chr8:65491800-65493000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:65491800-65494600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:65491800-65496000	Bivalent/Poised TSS	Fetal Brain Female	brain
8	chr8:65492000-65493000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr8:65492200-65493000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
10	chr8:65492200-65493000	Bivalent/Poised TSS	Right Ventricle	heart
11	chr8:65492200-65493000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
12	chr8:65492200-65493200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
13	chr8:65492200-65493200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
14	chr8:65492200-65493200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr8:65492200-65493200	Bivalent Enhancer	Fetal Lung	lung
16	chr8:65492200-65493200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
17	chr8:65492200-65494800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:65492200-65494800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
19	chr8:65492200-65494800	Active TSS	Right Atrium	heart
20	chr8:65492200-65495200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:65492400-65493000	Bivalent/Poised TSS	Colonic Mucosa	Colon
22	chr8:65492400-65493200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
23	chr8:65492400-65493400	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:65492400-65493400	Active TSS	Adipose Nuclei	Adipose
25	chr8:65492400-65493600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:65492400-65493800	Bivalent/Poised TSS	Psoas Muscle	Psoas
27	chr8:65492400-65494200	Active TSS	Brain Substantia Nigra	brain
28	chr8:65492400-65494200	Bivalent/Poised TSS	A549	lung
29	chr8:65492400-65494200	Active TSS	GM12878-XiMat	blood
30	chr8:65492400-65494400	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
31	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr8:65492600-65493000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:65492600-65493000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
35	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
36	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
37	chr8:65492600-65493000	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
39	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
40	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
41	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
42	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
43	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
45	chr8:65492600-65493000	Bivalent/Poised TSS	Fetal Brain Male	brain
46	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
47	chr8:65492600-65493000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
48	chr8:65492600-65493000	Bivalent/Poised TSS	NHDF-Ad	bronchial
49	chr8:65492600-65493200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:65492600-65493200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin

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