Variant report

Variant	nsv1032976
Chromosome Location	chr8:118032075-118065907
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	chr8:118056998-118057173	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:118056971-118057168	K562	blood:	n/a	n/a
3	CEBPB	chr8:118061644-118061729	A549	lung:	n/a	n/a
4	CEBPB	chr8:118053547-118053583	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr8:118046948-118047300	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr8:118032015-118032280	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr8:118045572-118046377	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:118031502-118032316	Hela-S3	cervix:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
9	CEBPB	chr8:118045665-118045911	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:118045623-118045693	A549	lung:	n/a	n/a
11	CEBPB	chr8:118031649-118032296	IMR90	lung:	n/a	chr8:118031801-118031812 chr8:118031678-118031689 chr8:118031676-118031689 chr8:118031678-118031689
12	CHD1	chr8:118047103-118047133	GM12878	blood:	n/a	n/a
13	CHD1	chr8:118046933-118047301	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr8:118057079-118057182	HepG2	liver:	n/a	n/a
15	CHD2	chr8:118047102-118047115	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr8:118057003-118057209	A549	lung:	n/a	n/a
17	CTCF	chr8:118050220-118050370	HRPEpiC	eye:	n/a	chr8:118050294-118050315
18	CTCF	chr8:118057020-118057170	GM12801	blood:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
19	CTCF	chr8:118050240-118050390	HUVEC	blood vessel:	n/a	chr8:118050294-118050315
20	CTCF	chr8:118050240-118050390	NHLF	lung:	n/a	chr8:118050294-118050315
21	CTCF	chr8:118057060-118057210	WERI-Rb-1	eye:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
22	CTCF	chr8:118050240-118050390	HPF	lung:	n/a	chr8:118050294-118050315
23	CTCF	chr8:118045141-118045210	GM20000	blood:	n/a	n/a
24	CTCF	chr8:118056979-118057263	HUVEC	blood vessel:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
25	CTCF	chr8:118057027-118057264	Kidney_OC	kidney:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
26	CTCF	chr8:118049960-118050110	GM12872	blood:	n/a	n/a
27	CTCF	chr8:118050220-118050370	AG10803	skin:	n/a	chr8:118050294-118050315
28	CTCF	chr8:118057060-118057210	AG09309	skin:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
29	CTCF	chr8:118057060-118057210	GM12868	blood:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
30	CTCF	chr8:118057080-118057230	GM12870	blood:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
31	CTCF	chr8:118050240-118050390	HPAF	blood vessel:	n/a	chr8:118050294-118050315
32	CTCF	chr8:118057020-118057170	SAEC	small airway:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
33	CTCF	chr8:118057060-118057210	GM12871	blood:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
34	CTCF	chr8:118057020-118057170	NHLF	lung:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
35	CTCF	chr8:118057040-118057190	HCPEpiC	choroid plexus:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
36	CTCF	chr8:118057040-118057190	HCM	heart:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
37	CTCF	chr8:118050251-118050370	GM13977	blood:	n/a	chr8:118050294-118050315
38	CTCF	chr8:118050220-118050370	K562	blood:	n/a	chr8:118050294-118050315
39	CTCF	chr8:118050228-118050326	GM13976	blood:	n/a	chr8:118050294-118050315
40	CTCF	chr8:118056999-118057266	GM10266	blood:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
41	CTCF	chr8:118057060-118057210	HRPEpiC	eye:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
42	CTCF	chr8:118050240-118050390	AG10803	skin:	n/a	chr8:118050294-118050315
43	CTCF	chr8:118050240-118050390	MCF-7	breast:	n/a	chr8:118050294-118050315
44	CTCF	chr8:118056522-118057512	A549	lung:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
45	CTCF	chr8:118056950-118057218	A549	lung:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
46	CTCF	chr8:118057004-118057260	GM13977	blood:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
47	CTCF	chr8:118056890-118057453	HCT-116	colon:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
48	CTCF	chr8:118050260-118050410	HFF	foreskin:	n/a	chr8:118050294-118050315
49	CTCF	chr8:118057040-118057190	HPF	lung:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133
50	CTCF	chr8:118057040-118057190	AG09319	gingival:	n/a	chr8:118057111-118057132 chr8:118057116-118057134 chr8:118057108-118057121 chr8:118057117-118057133

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:118057038-118057088	T-47D	breast:	n/a
2	chr8:118057038-118057088	HepG2	liver:	n/a
3	chr8:118057038-118057088	HUVEC	blood vessel:	n/a
4	chr8:118057038-118057088	H1-hESC	embryonic stem cell:	embryo
5	chr8:118057038-118057088	NB4	blood:	n/a
6	chr8:118057038-118057088	LNCaP	prostate:	n/a
7	chr8:118057038-118057088	Hepatocyte	liver:	n/a
8	chr8:118057038-118057088	A549	lung:	n/a
9	chr8:118057038-118057088	HEEpiC	esophagus:	n/a
10	chr8:118057038-118057088	HL-60	blood:	n/a
11	chr8:118057038-118057088	AoSMC	blood vessel:	n/a
12	chr8:118057038-118057088	GM12878	blood:	n/a
13	chr8:118057038-118057088	ovcar-3	ovarian:	n/a
14	chr8:118057038-118057088	HRCEpiC	kidney:	n/a
15	chr8:118057038-118057088	GM19239	blood:	n/a
16	chr8:118057038-118057088	HMEC	breast:	n/a
17	chr8:118057038-118057088	SK-N-SH_RA	brain:	n/a
18	chr8:118057038-118057088	ProgFib	skin:	n/a
19	chr8:118057038-118057088	SKMC	muscle:	n/a
20	chr8:118057038-118057088	NH-A	brain:	n/a
21	chr8:118057038-118057088	K562	blood:	n/a
22	chr8:118057038-118057088	SK-N-MC	brain:	n/a
23	chr8:118057038-118057088	NHDF-neo	bronchial:	n/a
24	chr8:118057038-118057088	U87	brain:	n/a
25	chr8:118057038-118057088	HAEpiC	amniotic membrane:	n/a
26	chr8:118057038-118057088	HRE	kidney:	n/a
27	chr8:118057038-118057088	MCF-7	breast:	n/a
28	chr8:118057038-118057088	AG04449	skin:	fetal
29	chr8:118057038-118057088	HCF	heart:	n/a
30	chr8:118057038-118057088	NT2-D1	testis:	n/a
31	chr8:118057038-118057088	HIPEpiC	eye:	n/a
32	chr8:118057038-118057088	SAEC	small airway:	n/a
33	chr8:118057038-118057088	AG04450	lung:	fetal
34	chr8:118057038-118057088	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:118057038-118057088	ECC-1	luminal epithelium:	n/a
36	chr8:118057038-118057088	Caco-2	colon:	n/a
37	chr8:118057038-118057088	PFSK-1	brain:	n/a
38	chr8:118057038-118057088	SK-N-SH	brain:	n/a
39	chr8:118057038-118057088	GM06990	blood:	n/a
40	chr8:118057038-118057088	Hela-S3	cervix:	n/a
41	chr8:118057038-118057088	RPTEC	kidney:	n/a
42	chr8:118057038-118057088	CMK	blood:	n/a
43	chr8:118057038-118057088	NHBE	bronchial:	n/a
44	chr8:118057038-118057088	GM12891	blood:	n/a
45	chr8:118057038-118057088	MCF10A-Er-Src	breast:	n/a
46	chr8:118057038-118057088	GM12892	blood:	n/a
47	chr8:118057038-118057088	AG09319	gingival:	n/a
48	chr8:118057038-118057088	PrEC	prostate:	n/a
49	chr8:118057038-118057088	AG10803	skin:	n/a
50	chr8:118057038-118057088	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:117798759..117799449-chr8:118050248..118050771,2	K562	blood:
2	chr8:117939124..117940068-chr8:118056652..118057163,2	K562	blood:
3	chr8:117965975..117966904-chr8:118049849..118050385,2	MCF-7	breast:
4	chr8:118043645..118045454-chr8:118048190..118050683,2	MCF-7	breast:
5	chr8:117899655..117900529-chr8:118049522..118050469,2	MCF-7	breast:
6	chr8:117938653..117939378-chr8:118056475..118057163,2	MCF-7	breast:
7	chr8:117939213..117940140-chr8:118049488..118050102,2	MCF-7	breast:
8	chr8:118049690..118050513-chr8:118316119..118316774,2	MCF-7	breast:
9	chr8:117863158..117863821-chr8:118056751..118057499,2	MCF-7	breast:
10	chr8:117800389..117801053-chr8:118056632..118057180,2	K562	blood:
11	chr8:117862359..117862912-chr8:118049512..118050408,2	MCF-7	breast:
12	chr8:118043645..118045454-chr8:118048190..118050683,2	MCF-7	breast:
13	chr8:117939530..117940032-chr8:118056656..118057269,2	MCF-7	breast:
14	chr8:118042679..118044189-chr9:110363714..110366279,2	MCF-7	breast:
15	chr8:118056632..118057588-chr8:118316103..118316951,2	MCF-7	breast:
16	chr8:118057127..118057700-chr8:118316063..118316814,2	K562	blood:
17	chr8:117939006..117940094-chr8:118049813..118050710,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253271	TF binding region
ENSG00000253271	CpG island

Extended variants
information (count: 1247 )
Associated
traits (count: 136 )

Variant overlapped rSNPs/rCNVs (count:1247 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371538642	chr8:118032100-118032101	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs558226195	chr8:118032132-118032133	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs10429430	chr8:118032189-118032190	Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs184514955	chr8:118032224-118032225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559305230	chr8:118032378-118032379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs151236832	chr8:118032406-118032407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542556122	chr8:118032417-118032418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140505287	chr8:118032442-118032443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559708994	chr8:118032572-118032573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376011333	chr8:118032597-118032598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531107719	chr8:118032624-118032625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189745115	chr8:118032689-118032690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150421258	chr8:118032827-118032828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537258226	chr8:118032844-118032845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181401817	chr8:118032849-118032850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546646927	chr8:118032890-118032891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149385315	chr8:118032909-118032910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150856000	chr8:118032910-118032911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79257878	chr8:118032911-118032912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138294651	chr8:118032924-118032925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200129385	chr8:118032938-118032939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373290195	chr8:118032947-118032948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568038478	chr8:118033004-118033005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535512238	chr8:118033047-118033048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184560529	chr8:118033067-118033068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569660903	chr8:118033075-118033076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115007703	chr8:118033131-118033132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572080959	chr8:118033142-118033143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189538674	chr8:118033159-118033160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180718869	chr8:118033174-118033175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537195204	chr8:118033178-118033179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116666181	chr8:118033184-118033185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562294875	chr8:118033214-118033215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552659987	chr8:118033218-118033219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574358902	chr8:118033306-118033307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10505292	chr8:118033327-118033328	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs563970413	chr8:118033337-118033338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570385143	chr8:118033341-118033342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13251837	chr8:118033360-118033361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549194952	chr8:118033362-118033363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564722896	chr8:118033371-118033372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75890618	chr8:118033379-118033380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs60860533	chr8:118033449-118033450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558797418	chr8:118033483-118033484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547053818	chr8:118033573-118033574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186385500	chr8:118033617-118033618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57977435	chr8:118033687-118033688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75736251	chr8:118033695-118033696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190884341	chr8:118033748-118033749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76010012	chr8:118033762-118033763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:136)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17268525	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	19204574	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118031400-118032200	Enhancers	Hela-S3	cervix
2	chr8:118031400-118032400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:118031400-118032400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:118031400-118032400	Enhancers	HSMMtube	muscle
5	chr8:118031600-118032200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr8:118031600-118032400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr8:118031600-118032400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr8:118031600-118032400	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr8:118031800-118032200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr8:118031800-118032200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr8:118031800-118032200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr8:118031800-118032200	Flanking Active TSS	Fetal Heart	heart
13	chr8:118031800-118032200	Bivalent Enhancer	Fetal Lung	lung
14	chr8:118031800-118032400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr8:118031800-118032400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:118031800-118032400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:118031800-118032400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:118031800-118032400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:118031800-118032400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:118031800-118032400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:118031800-118032400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr8:118031800-118032400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:118031800-118032400	Enhancers	Stomach Smooth Muscle	stomach
24	chr8:118031800-118032400	Enhancers	HSMM	muscle
25	chr8:118032000-118032400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr8:118032000-118032400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr8:118032000-118032400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr8:118032000-118032400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:118032200-118032400	Enhancers	Fetal Heart	heart
30	chr8:118032400-118037200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:118037200-118038600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:118038000-118038200	Enhancers	Psoas Muscle	Psoas
33	chr8:118038200-118038400	Enhancers	Rectal Smooth Muscle	rectum
34	chr8:118038200-118040600	Weak transcription	Psoas Muscle	Psoas
35	chr8:118038400-118040400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr8:118039200-118039600	Bivalent Enhancer	Right Atrium	heart
37	chr8:118039400-118039800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr8:118040400-118040800	Enhancers	Rectal Smooth Muscle	rectum
39	chr8:118040600-118040800	Enhancers	Psoas Muscle	Psoas
40	chr8:118040800-118045000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr8:118044800-118045400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr8:118045000-118045800	Enhancers	Rectal Smooth Muscle	rectum
43	chr8:118045000-118046400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:118045000-118046400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr8:118045000-118046600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:118045200-118045600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:118045200-118046200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr8:118045200-118046200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:118045200-118046200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr8:118045200-118046400	Enhancers	HMEC	breast

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