Variant report

Variant	nsv891234
Chromosome Location	chr8:103020391-103113701
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:835)
CpG islands
(count:184)
Chromatin interactive
region (count:69)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:103022217-103022485	K562	blood:	n/a	n/a
2	ATF1	chr8:103022145-103022506	K562	blood:	n/a	n/a
3	ATF1	chr8:103022862-103023130	K562	blood:	n/a	n/a
4	ATF1	chr8:103076282-103076533	K562	blood:	n/a	n/a
5	ATF2	chr8:103109852-103110464	GM12878	blood:	n/a	n/a
6	BATF	chr8:103064832-103065087	GM12878	blood:	n/a	chr8:103064987-103064998
7	BATF	chr8:103051921-103052148	GM12878	blood:	n/a	n/a
8	BATF	chr8:103110056-103110409	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:103110000-103110286	GM12878	blood:	n/a	chr8:103110218-103110227
10	BCL11A	chr8:103108741-103109093	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:103108706-103109105	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:103109974-103110337	GM12878	blood:	n/a	chr8:103110218-103110227
13	BCL11A	chr8:103057235-103057588	GM12878	blood:	n/a	chr8:103057382-103057391
14	BCL11A	chr8:103057263-103057535	GM12878	blood:	n/a	chr8:103057382-103057391
15	BHLHE40	chr8:103057292-103057491	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:103113281-103113436	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:103022193-103022314	K562	blood:	n/a	n/a
18	BHLHE40	chr8:103113374-103113458	K562	blood:	n/a	n/a
19	BHLHE40	chr8:103109904-103110471	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:103108681-103109042	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:103078732-103079055	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:103109385-103109584	GM12878	blood:	n/a	n/a
23	CBX3	chr8:103065585-103065884	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:103102840-103103050	K562	blood:	n/a	n/a
25	CBX3	chr8:103022259-103022573	K562	blood:	n/a	n/a
26	CBX3	chr8:103022179-103022648	K562	blood:	n/a	n/a
27	CBX3	chr8:103024659-103024984	K562	blood:	n/a	n/a
28	CCNT2	chr8:103022224-103022452	K562	blood:	n/a	n/a
29	CCNT2	chr8:103077410-103077481	K562	blood:	n/a	n/a
30	CEBPB	chr8:103113125-103113312	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:103078708-103078915	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr8:103109726-103110535	GM12878	blood:	n/a	n/a
33	CEBPB	chr8:103078473-103078974	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr8:103113098-103113327	A549	lung:	n/a	n/a
35	CEBPB	chr8:103113100-103113347	K562	blood:	n/a	n/a
36	CEBPB	chr8:103024739-103024794	A549	lung:	n/a	n/a
37	CEBPB	chr8:103078237-103079091	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr8:103057857-103058627	ECC-1	luminal epithelium:	n/a	chr8:103058162-103058173
39	CEBPB	chr8:103094504-103094905	ECC-1	luminal epithelium:	n/a	chr8:103094694-103094705 chr8:103094692-103094705 chr8:103094694-103094705 chr8:103094692-103094705
40	CEBPB	chr8:103083638-103083841	HepG2	liver:	n/a	chr8:103083727-103083738
41	CEBPB	chr8:103083602-103083781	A549	lung:	n/a	chr8:103083727-103083738
42	CEBPB	chr8:103057964-103058536	ECC-1	luminal epithelium:	n/a	chr8:103058162-103058173
43	CEBPB	chr8:103104759-103104923	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:103027533-103027827	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:103083610-103083907	K562	blood:	n/a	chr8:103083727-103083738
46	CEBPB	chr8:103059117-103059209	A549	lung:	n/a	n/a
47	CEBPB	chr8:103113138-103113327	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:103022278-103022615	K562	blood:	n/a	n/a
49	CEBPB	chr8:103027539-103027652	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:103094582-103094879	ECC-1	luminal epithelium:	n/a	chr8:103094694-103094705 chr8:103094692-103094705 chr8:103094694-103094705 chr8:103094692-103094705

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103094119-103094169	AG10803	skin:	n/a
2	chr8:103094119-103094169	AG10803	skin:	n/a
3	chr8:103094119-103094169	Hepatocyte	liver:	n/a
4	chr8:103094119-103094169	K562	blood:	n/a
5	chr8:103035373-103035423	GM12891	blood:	n/a
6	chr8:103035373-103035423	U87	brain:	n/a
7	chr8:103113436-103113486	T-47D	breast:	n/a
8	chr8:103035373-103035423	HRCEpiC	kidney:	n/a
9	chr8:103035373-103035423	RPTEC	kidney:	n/a
10	chr8:103035373-103035423	PFSK-1	brain:	n/a
11	chr8:103113436-103113486	HIPEpiC	eye:	n/a
12	chr8:103035373-103035423	AoSMC	blood vessel:	n/a
13	chr8:103094119-103094169	SK-N-MC	brain:	n/a
14	chr8:103035373-103035423	PANC-1	pancreas:	n/a
15	chr8:103113436-103113486	HCM	heart:	n/a
16	chr8:103094119-103094169	HRPEpiC	eye:	n/a
17	chr8:103035373-103035423	HCT-116	colon:	n/a
18	chr8:103035373-103035423	HPAEpiC	pulmonary alveolar:	n/a
19	chr8:103094119-103094169	Hela-S3	cervix:	n/a
20	chr8:103035373-103035423	Hela-S3	cervix:	n/a
21	chr8:103094119-103094169	NB4	blood:	n/a
22	chr8:103035373-103035423	H1-hESC	embryonic stem cell:	embryo
23	chr8:103035373-103035423	SAEC	small airway:	n/a
24	chr8:103113436-103113486	PFSK-1	brain:	n/a
25	chr8:103094119-103094169	GM12891	blood:	n/a
26	chr8:103035373-103035423	Caco-2	colon:	n/a
27	chr8:103035373-103035423	GM12892	blood:	n/a
28	chr8:103113436-103113486	SK-N-SH_RA	brain:	n/a
29	chr8:103113436-103113486	GM06990	blood:	n/a
30	chr8:103113436-103113486	GM19239	blood:	n/a
31	chr8:103035373-103035423	HAEpiC	amniotic membrane:	n/a
32	chr8:103035373-103035423	HepG2	liver:	n/a
33	chr8:103094119-103094169	RPTEC	kidney:	n/a
34	chr8:103035373-103035423	ovcar-3	ovarian:	n/a
35	chr8:103094119-103094169	GM06990	blood:	n/a
36	chr8:103113436-103113486	ECC-1	luminal epithelium:	n/a
37	chr8:103113436-103113486	RPTEC	kidney:	n/a
38	chr8:103094119-103094169	ECC-1	luminal epithelium:	n/a
39	chr8:103113436-103113486	SAEC	small airway:	n/a
40	chr8:103113436-103113486	HCPEpiC	choroid plexus:	n/a
41	chr8:103035373-103035423	NHDF-neo	bronchial:	n/a
42	chr8:103094119-103094169	PrEC	prostate:	n/a
43	chr8:103094119-103094169	AG09309	skin:	n/a
44	chr8:103094119-103094169	HCT-116	colon:	n/a
45	chr8:103035373-103035423	GM19239	blood:	n/a
46	chr8:103094119-103094169	HEEpiC	esophagus:	n/a
47	chr8:103035373-103035423	MCF-7	breast:	n/a
48	chr8:103094119-103094169	GM12892	blood:	n/a
49	chr8:103035373-103035423	K562	blood:	n/a
50	chr8:103035373-103035423	NH-A	brain:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:103103923..103106392-chr8:103121808..103124268,2	MCF-7	breast:
2	chr8:103072599..103074575-chr8:103077448..103079035,2	MCF-7	breast:
3	chr8:103089569..103093166-chr8:103094266..103096675,3	K562	blood:
4	chr8:103045659..103047816-chr8:103052482..103055042,2	MCF-7	breast:
5	chr8:103053043..103055176-chr8:103059742..103061344,2	MCF-7	breast:
6	chr8:103084257..103086284-chr8:103112303..103114668,2	MCF-7	breast:
7	chr8:94657213..94658713-chr8:103102291..103104933,2	MCF-7	breast:
8	chr8:103053043..103055176-chr8:103059742..103061344,2	MCF-7	breast:
9	chr8:103086669..103088305-chr8:103090497..103092888,2	K562	blood:
10	chr8:103044680..103045636-chr8:103079751..103080379,3	MCF-7	breast:
11	chr8:103040180..103042383-chr8:103042773..103045419,2	K562	blood:
12	chr8:103025621..103028560-chr8:103033345..103035115,2	MCF-7	breast:
13	chr8:103086669..103088305-chr8:103090497..103092888,2	K562	blood:
14	chr8:103111624..103115089-chr8:103119935..103122230,3	MCF-7	breast:
15	chr8:103089569..103092563-chr8:103094266..103096164,2	K562	blood:
16	chr8:103112507..103115331-chr8:103120087..103122301,2	K562	blood:
17	chr8:103044931..103046316-chr8:103209230..103210787,8	MCF-7	breast:
18	chr8:103100572..103102225-chr8:103104535..103106476,2	MCF-7	breast:
19	chr8:103044933..103045692-chr8:103135558..103136538,3	MCF-7	breast:
20	chr8:103018598..103021220-chr8:103040638..103042919,2	MCF-7	breast:
21	chr8:103037680..103039955-chr8:103043079..103045109,2	K562	blood:
22	chr8:103072599..103074575-chr8:103077448..103079035,2	MCF-7	breast:
23	chr8:103062774..103065761-chr8:103066216..103068204,2	K562	blood:
24	chr8:103073305..103075976-chr8:103083458..103085206,2	K562	blood:
25	chr7:142098691..142099254-chr8:103045443..103046063,2	MCF-7	breast:
26	chr8:103049817..103051629-chr8:103058338..103060575,3	MCF-7	breast:
27	chr8:103082278..103084453-chr8:103115939..103117501,2	MCF-7	breast:
28	chr8:103017031..103018627-chr8:103042578..103044684,2	K562	blood:
29	chr8:103040180..103042383-chr8:103042773..103045419,2	K562	blood:
30	chr8:103089569..103093166-chr8:103094266..103096675,3	K562	blood:
31	chr8:103044680..103045636-chr8:103079751..103080379,3	MCF-7	breast:
32	chr8:103104191..103106408-chr8:103110112..103111638,2	MCF-7	breast:
33	chr8:103054616..103056405-chr8:103111193..103113703,2	MCF-7	breast:
34	chr8:103084929..103087953-chr8:103089291..103092188,3	MCF-7	breast:
35	chr8:103054616..103056405-chr8:103111193..103113703,2	MCF-7	breast:
36	chr8:103105888..103108288-chr8:103119187..103121586,2	MCF-7	breast:
37	chr8:103045659..103047816-chr8:103052482..103055042,2	MCF-7	breast:
38	chr8:103023024..103025926-chr8:103825006..103827127,2	K562	blood:
39	chr8:103077871..103079434-chr8:103084965..103087880,2	K562	blood:
40	chr8:103073305..103075976-chr8:103083458..103085206,2	K562	blood:
41	chr8:103025621..103028560-chr8:103033345..103035115,2	MCF-7	breast:
42	chr8:103002460..103004143-chr8:103021430..103023271,2	K562	blood:
43	chr8:103032420..103035113-chr8:103035889..103038603,2	MCF-7	breast:
44	chr8:103077871..103079434-chr8:103084965..103087880,2	K562	blood:
45	chr8:103104191..103106408-chr8:103110112..103111638,2	MCF-7	breast:
46	chr8:103065341..103067614-chr8:103067758..103069814,2	MCF-7	breast:
47	chr8:103095933..103097861-chr8:103100230..103102303,2	MCF-7	breast:
48	chr8:102658411..102659082-chr8:103044751..103045545,2	MCF-7	breast:
49	chr8:103092184..103094951-chr8:103097737..103099786,2	MCF-7	breast:
50	chr8:103095933..103097861-chr8:103100230..103102303,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRM2B-8	chr8:103032465-103032517	NONHSAT128070
2	lnc-RRM2B-8	chr8:103032465-103032517	NONHSAT128075

No data

Variant related genes	Relation type
NCALD	TF binding region
NCALD	CpG island
ENSG00000253781	chromatin interactions
ENSG00000104490	chromatin interactions

Extended variants
information (count: 3262 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:3262 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1351063	chr8:103020391-103020392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2387330	chr8:103020432-103020433	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs148794146	chr8:103020596-103020597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74417367	chr8:103020644-103020645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142461633	chr8:103020645-103020646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150811380	chr8:103020646-103020647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182680222	chr8:103020674-103020675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531026423	chr8:103020698-103020699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34867950	chr8:103020702-103020703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71268538	chr8:103020720-103020721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549538055	chr8:103020722-103020723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568089634	chr8:103020776-103020777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367583818	chr8:103020836-103020837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139263706	chr8:103020901-103020902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533391331	chr8:103020904-103020905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551781709	chr8:103020926-103020927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11776916	chr8:103020951-103020952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539412829	chr8:103020956-103020957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372462018	chr8:103020984-103020985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs80104106	chr8:103020991-103020992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187010796	chr8:103021023-103021024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74451501	chr8:103021036-103021037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370271041	chr8:103021062-103021063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556194353	chr8:103021127-103021128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536879498	chr8:103021132-103021133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201563851	chr8:103021138-103021139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371738780	chr8:103021146-103021147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60824028	chr8:103021196-103021197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192219466	chr8:103021197-103021198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71518844	chr8:103021201-103021202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555538016	chr8:103021209-103021210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573840521	chr8:103021248-103021249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541134445	chr8:103021282-103021283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146571365	chr8:103021292-103021293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577634965	chr8:103021298-103021299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566992796	chr8:103021324-103021325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200685071	chr8:103021382-103021383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201571922	chr8:103021383-103021384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545350769	chr8:103021404-103021405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182839723	chr8:103021422-103021423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188534387	chr8:103021436-103021437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141323159	chr8:103021451-103021452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144093717	chr8:103021461-103021462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11777031	chr8:103021465-103021466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11783903	chr8:103021475-103021476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs546920606	chr8:103021527-103021528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565485263	chr8:103021640-103021641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs193124183	chr8:103021661-103021662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146489117	chr8:103021699-103021700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532990656	chr8:103021721-103021722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22495309	CNVD

Chromatin state (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103010200-103028400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr8:103010400-103022800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:103010400-103027200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr8:103010800-103028400	Weak transcription	Aorta	Aorta
5	chr8:103012600-103024600	Weak transcription	Ovary	ovary
6	chr8:103013000-103024200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:103017600-103024200	Weak transcription	Primary T cells from cord blood	blood
8	chr8:103019000-103024200	Weak transcription	Left Ventricle	heart
9	chr8:103019200-103025600	Weak transcription	Right Ventricle	heart
10	chr8:103020000-103020600	Enhancers	Psoas Muscle	Psoas
11	chr8:103020200-103022000	Enhancers	K562	blood
12	chr8:103020200-103023200	Weak transcription	Fetal Heart	heart
13	chr8:103020200-103023200	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr8:103020200-103024200	Weak transcription	Fetal Muscle Leg	muscle
15	chr8:103020600-103022200	Weak transcription	Psoas Muscle	Psoas
16	chr8:103022000-103022200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:103022000-103022600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr8:103022000-103022600	Flanking Active TSS	K562	blood
19	chr8:103022000-103023000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr8:103022200-103022400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr8:103022200-103022400	Enhancers	Lung	lung
22	chr8:103022200-103022400	Enhancers	Right Atrium	heart
23	chr8:103022200-103022600	Enhancers	Psoas Muscle	Psoas
24	chr8:103022200-103027000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:103022400-103022600	Enhancers	Placenta	Placenta
26	chr8:103022400-103023000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr8:103022400-103024600	Weak transcription	Lung	lung
28	chr8:103022400-103025600	Weak transcription	Right Atrium	heart
29	chr8:103022400-103028600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr8:103022600-103022800	Enhancers	K562	blood
31	chr8:103022600-103024200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr8:103022600-103025400	Weak transcription	Psoas Muscle	Psoas
33	chr8:103022800-103023200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:103022800-103023600	Flanking Active TSS	K562	blood
35	chr8:103022800-103024200	Weak transcription	Placenta	Placenta
36	chr8:103023000-103028200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr8:103023200-103023600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr8:103023200-103024600	Enhancers	Fetal Heart	heart
39	chr8:103023200-103027800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:103023600-103024200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr8:103023600-103025000	Enhancers	K562	blood
42	chr8:103024200-103024400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr8:103024200-103024600	Strong transcription	Primary T cells from cord blood	blood
44	chr8:103024200-103024800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:103024200-103024800	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr8:103024200-103025000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr8:103024200-103025000	Enhancers	Placenta	Placenta
48	chr8:103024200-103025200	Enhancers	Left Ventricle	heart
49	chr8:103024200-103025600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:103024200-103026000	Enhancers	Fetal Muscle Leg	muscle

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