Variant report

Variant	nsv467718
Chromosome Location	chr11:17744992-17809724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1792)
CpG islands
(count:2259)
Chromatin interactive
region (count:84)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1792 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17791527-17791963	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:17752734-17752850	HepG2	liver:	n/a	n/a
3	ATF1	chr11:17783928-17784200	K562	blood:	n/a	n/a
4	BACH1	chr11:17781712-17781838	K562	blood:	n/a	n/a
5	BACH1	chr11:17756192-17756315	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:17808619-17808727	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:17781684-17782192	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr11:17756573-17756763	GM12878	blood:	n/a	chr11:17756644-17756660
9	BHLHE40	chr11:17799360-17799604	K562	blood:	n/a	n/a
10	BHLHE40	chr11:17752607-17752898	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:17791512-17792072	HepG2	liver:	n/a	n/a
12	BHLHE40	chr11:17756560-17756818	HepG2	liver:	n/a	chr11:17756644-17756660
13	BHLHE40	chr11:17756580-17756727	K562	blood:	n/a	chr11:17756644-17756660
14	BHLHE40	chr11:17782021-17782165	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:17781973-17782310	K562	blood:	n/a	n/a
16	BHLHE40	chr11:17784019-17784137	K562	blood:	n/a	n/a
17	BHLHE40	chr11:17791514-17791889	K562	blood:	n/a	n/a
18	BRCA1	chr11:17752601-17752887	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr11:17781963-17782291	HepG2	liver:	n/a	n/a
20	BRCA1	chr11:17752773-17752833	GM12878	blood:	n/a	n/a
21	BRCA1	chr11:17752729-17752836	HepG2	liver:	n/a	n/a
22	CBX3	chr11:17791632-17791866	K562	blood:	n/a	n/a
23	CBX3	chr11:17781908-17782256	K562	blood:	n/a	n/a
24	CEBPB	chr11:17756623-17756736	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:17772452-17772532	H1-hESC	embryonic stem cell:	n/a	chr11:17772511-17772522
26	CEBPB	chr11:17772343-17772697	HepG2	liver:	n/a	chr11:17772511-17772522
27	CEBPB	chr11:17772354-17772618	HepG2	liver:	n/a	chr11:17772511-17772522
28	CEBPB	chr11:17776105-17776129	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:17772409-17772648	HepG2	liver:	n/a	chr11:17772511-17772522
30	CEBPB	chr11:17779188-17779456	IMR90	lung:	n/a	chr11:17779294-17779305
31	CEBPB	chr11:17752652-17752914	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:17772414-17772625	Hela-S3	cervix:	n/a	chr11:17772511-17772522
33	CEBPB	chr11:17791598-17791899	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:17779238-17779303	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:17782011-17782346	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:17772348-17772662	HepG2	liver:	n/a	chr11:17772511-17772522
37	CEBPB	chr11:17752665-17752866	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:17772512-17772518	K562	blood:	n/a	n/a
39	CEBPB	chr11:17752607-17752941	Hela-S3	cervix:	n/a	n/a
40	CEBPD	chr11:17791540-17791900	HepG2	liver:	n/a	n/a
41	CHD1	chr11:17752489-17753087	IMR90	lung:	n/a	n/a
42	CHD1	chr11:17752611-17752799	GM12878	blood:	n/a	n/a
43	CHD1	chr11:17756611-17756687	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr11:17781920-17782286	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr11:17782199-17782328	K562	blood:	n/a	n/a
46	CHD2	chr11:17756640-17756806	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr11:17791574-17791809	K562	blood:	n/a	n/a
48	CHD2	chr11:17791517-17791901	HepG2	liver:	n/a	n/a
49	CHD2	chr11:17752390-17752860	GM12878	blood:	n/a	n/a
50	CHD2	chr11:17757402-17757762	H1-hESC	embryonic stem cell:	n/a	chr11:17757442-17757452

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17803421-17803471	LNCaP	prostate:	n/a
2	chr11:17803369-17803419	K562	blood:	n/a
3	chr11:17803421-17803471	LNCaP	prostate:	n/a
4	chr11:17803369-17803419	K562	blood:	n/a
5	chr11:17799117-17799167	HMEC	breast:	n/a
6	chr11:17798912-17798962	Hela-S3	cervix:	n/a
7	chr11:17796490-17796540	GM19239	blood:	n/a
8	chr11:17793350-17793400	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:17803389-17803439	MCF10A-Er-Src	breast:	n/a
10	chr11:17756435-17756485	ECC-1	luminal epithelium:	n/a
11	chr11:17757129-17757179	NHDF-neo	bronchial:	n/a
12	chr11:17803369-17803419	GM12891	blood:	n/a
13	chr11:17803369-17803419	CMK	blood:	n/a
14	chr11:17760574-17760624	Hepatocyte	liver:	n/a
15	chr11:17757129-17757179	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:17756479-17756529	Jurkat	blood:	n/a
17	chr11:17790285-17790335	HRPEpiC	eye:	n/a
18	chr11:17799117-17799167	HCM	heart:	n/a
19	chr11:17756986-17757036	Hepatocyte	liver:	n/a
20	chr11:17765568-17765618	CMK	blood:	n/a
21	chr11:17791761-17791811	AG09319	gingival:	n/a
22	chr11:17793350-17793400	AG04450	lung:	fetal
23	chr11:17761718-17761768	HepG2	liver:	n/a
24	chr11:17799117-17799167	H1-hESC	embryonic stem cell:	embryo
25	chr11:17801276-17801326	ProgFib	skin:	n/a
26	chr11:17790285-17790335	AG09319	gingival:	n/a
27	chr11:17796490-17796540	SAEC	small airway:	n/a
28	chr11:17801276-17801326	HIPEpiC	eye:	n/a
29	chr11:17765568-17765618	HEK293	kidney:	embryo
30	chr11:17793958-17794008	AG04449	skin:	fetal
31	chr11:17759573-17759623	MCF10A-Er-Src	breast:	n/a
32	chr11:17757415-17757465	AG09309	skin:	n/a
33	chr11:17798912-17798962	A549	lung:	n/a
34	chr11:17803389-17803439	HRE	kidney:	n/a
35	chr11:17759573-17759623	HRPEpiC	eye:	n/a
36	chr11:17793350-17793400	H1-hESC	embryonic stem cell:	embryo
37	chr11:17796490-17796540	HUVEC	blood vessel:	n/a
38	chr11:17758285-17758335	PrEC	prostate:	n/a
39	chr11:17756435-17756485	PrEC	prostate:	n/a
40	chr11:17803369-17803419	SK-N-SH	brain:	n/a
41	chr11:17756986-17757036	Caco-2	colon:	n/a
42	chr11:17803389-17803439	SK-N-SH	brain:	n/a
43	chr11:17756479-17756529	SKMC	muscle:	n/a
44	chr11:17760574-17760624	SAEC	small airway:	n/a
45	chr11:17765568-17765618	HCF	heart:	n/a
46	chr11:17758537-17758587	CMK	blood:	n/a
47	chr11:17791761-17791811	ECC-1	luminal epithelium:	n/a
48	chr11:17803160-17803210	H1-hESC	embryonic stem cell:	embryo
49	chr11:17756750-17756800	SK-N-SH_RA	brain:	n/a
50	chr11:17765568-17765618	ovcar-3	ovarian:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:17755705..17757483-chr11:17762543..17764877,2	K562	blood:
2	chr11:17791307..17792105-chr11:17946399..17946914,2	MCF-7	breast:
3	chr11:17781608..17782534-chr11:17926929..17928261,6	MCF-7	breast:
4	chr11:17791247..17794224-chr11:17800123..17802336,2	MCF-7	breast:
5	chr11:17804443..17806483-chr11:17873609..17875464,2	K562	blood:
6	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
7	chr11:17751921..17752763-chr19:36040271..36040795,2	MCF-7	breast:
8	chr11:17426978..17427915-chr11:17791365..17792205,5	MCF-7	breast:
9	chr11:17614764..17616023-chr11:17751704..17752684,3	MCF-7	breast:
10	chr11:17752210..17753037-chr11:17762564..17763159,2	K562	blood:
11	chr11:17781698..17782597-chr11:18001016..18002078,5	K562	blood:
12	chr11:17752210..17753037-chr11:17762564..17763159,2	K562	blood:
13	chr11:17790395..17791963-chr11:17795616..17797848,2	K562	blood:
14	chr11:17753668..17754453-chr6:57615850..57616702,2	MCF-7	breast:
15	chr11:17781544..17782571-chr11:17999973..18000867,4	K562	blood:
16	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
17	chr11:17588922..17590478-chr11:17766034..17768818,2	K562	blood:
18	chr11:17751795..17753232-chr11:17999934..18001786,19	MCF-7	breast:
19	chr11:17781701..17782562-chr11:17868027..17868986,3	MCF-7	breast:
20	chr11:17791549..17792453-chr11:17833752..17834540,3	MCF-7	breast:
21	chr11:17752483..17753383-chr11:17994354..17995164,3	MCF-7	breast:
22	chr11:17802511..17804986-chr11:17809141..17810811,2	K562	blood:
23	chr11:17778611..17780573-chr11:17781418..17783922,2	K562	blood:
24	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
25	chr11:17781589..17782577-chr11:17885405..17886255,2	K562	blood:
26	chr11:17781862..17782597-chr11:17994721..17995346,2	K562	blood:
27	chr11:17790395..17791963-chr11:17795616..17797848,2	K562	blood:
28	chr11:17764908..17766462-chr11:17767114..17769351,2	K562	blood:
29	chr11:17783515..17784102-chr11:17848668..17849177,2	MCF-7	breast:
30	chr11:17802032..17804366-chr11:17833882..17835723,2	MCF-7	breast:
31	chr11:17751864..17753212-chr11:17999973..18001949,7	MCF-7	breast:
32	chr11:17752292..17753246-chr11:17999986..18000903,4	K562	blood:
33	chr11:17752064..17753282-chr11:17994336..17995305,5	MCF-7	breast:
34	chr11:17788184..17788771-chr11:17801223..17802052,2	MCF-7	breast:
35	chr11:17768773..17771131-chr11:17771902..17774873,3	K562	blood:
36	chr11:17781843..17782605-chr11:17868062..17868630,2	MCF-7	breast:
37	chr11:17794271..17797051-chr11:17798441..17802132,3	K562	blood:
38	chr11:17781836..17782575-chr11:17999957..18000865,3	MCF-7	breast:
39	chr11:17789104..17793559-chr11:17796092..17800270,5	MCF-7	breast:
40	chr11:17757117..17759964-chr11:17765393..17768099,2	MCF-7	breast:
41	chr11:17752308..17752866-chr11:17774705..17775593,2	MCF-7	breast:
42	chr11:17789104..17793559-chr11:17796092..17800270,5	MCF-7	breast:
43	chr11:17620244..17621142-chr11:17752157..17753016,5	MCF-7	breast:
44	chr11:17781854..17784746-chr11:17785272..17786871,2	MCF-7	breast:
45	chr11:17752308..17753219-chr11:18785582..18786221,2	K562	blood:
46	chr11:17783850..17786298-chr11:17789626..17792965,4	K562	blood:
47	chr11:17791157..17792211-chr11:17946174..17946920,6	MCF-7	breast:
48	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
49	chr11:17781823..17782570-chr11:18001193..18001905,2	MCF-7	breast:
50	chr11:17622618..17623441-chr11:17752027..17752742,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERGEF-1	chr11:17809595-17809960	NONHSAT018248
2	lnc-SERGEF-1	chr11:17809599-17809960	NONHSAT018251
3	lnc-SERGEF-1	chr11:17809595-17809960	NONHSAT018250
4	lnc-MYOD1-2	chr11:17795943-17799369	NONHSAT018246
5	lnc-SERGEF-1	chr11:17809595-17809960	NONHSAT018249

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KCNC1	hsa-miR-335-5p	chr11:17803647-17803670

Variant related genes	Relation type
KCNC1	TF binding region
KCNC1	CpG island
ENSG00000129159	chromatin interactions

Extended variants
information (count: 2470 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2470 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3858511	chr11:17744992-17744993	Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529270531	chr11:17745029-17745030	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146456961	chr11:17745072-17745073	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4757585	chr11:17745099-17745100	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs560016392	chr11:17745115-17745116	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535980302	chr11:17745135-17745136	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184574045	chr11:17745160-17745161	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75926735	chr11:17745177-17745178	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570483319	chr11:17745181-17745182	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567559649	chr11:17745198-17745199	Bivalent Enhancer Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71484784	chr11:17745266-17745267	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190064098	chr11:17745300-17745301	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs193013239	chr11:17745301-17745302	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138932030	chr11:17745316-17745317	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72867874	chr11:17745338-17745339	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs149440386	chr11:17745374-17745375	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61880590	chr11:17745377-17745378	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370768399	chr11:17745382-17745383	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576738642	chr11:17745409-17745410	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566889105	chr11:17745421-17745422	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534046421	chr11:17745443-17745444	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547932137	chr11:17745444-17745445	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72867875	chr11:17745447-17745448	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs544188889	chr11:17745476-17745477	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556628814	chr11:17745485-17745486	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575051928	chr11:17745510-17745511	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542089723	chr11:17745514-17745515	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560752864	chr11:17745520-17745521	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538724483	chr11:17745625-17745626	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs36096028	chr11:17745626-17745627	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs545915734	chr11:17745644-17745645	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566154928	chr11:17745646-17745647	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148132824	chr11:17745685-17745686	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371443227	chr11:17745706-17745707	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531376145	chr11:17745720-17745721	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549746744	chr11:17745761-17745762	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561862502	chr11:17745762-17745763	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574738900	chr11:17745774-17745775	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547342940	chr11:17745786-17745787	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367818448	chr11:17745813-17745814	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565562160	chr11:17745824-17745825	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72867877	chr11:17745836-17745837	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs146201626	chr11:17745874-17745875	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570607145	chr11:17745950-17745951	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77719609	chr11:17745978-17745979	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556503048	chr11:17746037-17746038	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184798226	chr11:17746100-17746101	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536167446	chr11:17746114-17746115	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3858512	chr11:17746119-17746120	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs374846902	chr11:17746168-17746169	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17741800-17750200	Weak transcription	Right Atrium	heart
2	chr11:17744200-17745000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
3	chr11:17744200-17745600	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr11:17744200-17755400	Weak transcription	Psoas Muscle	Psoas
5	chr11:17744400-17745000	Strong transcription	Muscle Satellite Cultured Cells	--
6	chr11:17744600-17745000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:17744800-17745200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
8	chr11:17744800-17746600	Strong transcription	Fetal Muscle Trunk	muscle
9	chr11:17744800-17752400	Weak transcription	HSMM	muscle
10	chr11:17745000-17751600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:17745800-17746000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr11:17746000-17751600	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr11:17746600-17751800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr11:17747200-17752400	Weak transcription	Fetal Muscle Leg	muscle
15	chr11:17751600-17752000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
16	chr11:17751600-17753800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr11:17751800-17752000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr11:17751800-17752000	Genic enhancers	Fetal Muscle Trunk	muscle
19	chr11:17752000-17752200	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr11:17752000-17752400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr11:17752000-17752400	Enhancers	Hela-S3	cervix
22	chr11:17752000-17752800	Enhancers	Fetal Muscle Trunk	muscle
23	chr11:17752000-17753200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr11:17752200-17752400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
25	chr11:17752400-17752600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
26	chr11:17752400-17752600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
27	chr11:17752400-17752600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
28	chr11:17752400-17752600	Bivalent Enhancer	Fetal Intestine Large	intestine
29	chr11:17752400-17752600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
30	chr11:17752400-17752600	Flanking Active TSS	Hela-S3	cervix
31	chr11:17752400-17752600	Enhancers	HSMMtube	muscle
32	chr11:17752400-17752800	Enhancers	HSMM	muscle
33	chr11:17752400-17753000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:17752400-17753200	Enhancers	Fetal Muscle Leg	muscle
35	chr11:17752400-17753400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr11:17752600-17752800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
37	chr11:17752600-17752800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr11:17752600-17752800	Active TSS	Hela-S3	cervix
39	chr11:17752600-17754600	Weak transcription	HSMMtube	muscle
40	chr11:17752800-17753000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:17752800-17753000	Bivalent Enhancer	Fetal Stomach	stomach
42	chr11:17752800-17753200	Enhancers	Liver	Liver
43	chr11:17752800-17753400	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:17752800-17753400	Enhancers	Fetal Brain Male	brain
45	chr11:17752800-17753400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
46	chr11:17752800-17753600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr11:17752800-17755800	Weak transcription	HSMM	muscle
48	chr11:17753000-17753200	Enhancers	Fetal Brain Female	brain
49	chr11:17753200-17753400	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr11:17753200-17753600	Bivalent Enhancer	Liver	Liver

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