Variant report

Variant	nsv394
Chromosome Location	chr11:75820547-75865777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:831)
CpG islands
(count:488)
Chromatin interactive
region (count:42)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:831 , 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	chr11:75825160-75825598	K562	blood:	n/a	n/a
2	ARID3A	chr11:75864561-75864736	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:75860104-75860534	HepG2	liver:	n/a	n/a
4	BACH1	chr11:75863315-75863554	K562	blood:	n/a	n/a
5	BACH1	chr11:75863235-75863689	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:75845991-75845992	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:75863157-75863483	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:75859336-75859565	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:75826721-75826921	K562	blood:	n/a	n/a
10	BHLHE40	chr11:75863130-75863541	K562	blood:	n/a	n/a
11	BHLHE40	chr11:75863190-75864725	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:75863097-75863611	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:75864332-75864403	GM12878	blood:	n/a	n/a
14	BRCA1	chr11:75859962-75860259	HepG2	liver:	n/a	n/a
15	BRCA1	chr11:75863059-75863180	GM12878	blood:	n/a	n/a
16	BRCA1	chr11:75860608-75860664	HepG2	liver:	n/a	n/a
17	CBX3	chr11:75863136-75863522	K562	blood:	n/a	n/a
18	CBX3	chr11:75860471-75860754	K562	blood:	n/a	n/a
19	CBX3	chr11:75863093-75863564	K562	blood:	n/a	n/a
20	CEBPB	chr11:75863212-75863543	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr11:75864527-75864840	HepG2	liver:	n/a	n/a
22	CEBPB	chr11:75863232-75863509	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr11:75860136-75860449	HepG2	liver:	n/a	n/a
24	CHD1	chr11:75864059-75864324	GM12878	blood:	n/a	n/a
25	CHD1	chr11:75863452-75863569	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr11:75863280-75863634	GM12878	blood:	n/a	n/a
27	CHD2	chr11:75863193-75864849	GM12878	blood:	n/a	n/a
28	CHD2	chr11:75863228-75863475	HepG2	liver:	n/a	n/a
29	CHD2	chr11:75863222-75863456	K562	blood:	n/a	n/a
30	CHD2	chr11:75863065-75863567	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:75863212-75863531	Hela-S3	cervix:	n/a	n/a
32	CREB1	chr11:75863140-75863514	A549	lung:	n/a	n/a
33	CTCF	chr11:75830160-75830310	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr11:75830208-75830358	A549	lung:	n/a	n/a
35	CTCF	chr11:75827752-75827768	Medullo	brain:	n/a	n/a
36	CTCF	chr11:75863340-75863490	GM12865	blood:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
37	CTCF	chr11:75863249-75863561	Lung_OC	lung:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
38	CTCF	chr11:75863144-75863631	A549	lung:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
39	CTCF	chr11:75857815-75858068	IMR90	lung:	n/a	n/a
40	CTCF	chr11:75863320-75863470	GM06990	blood:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
41	CTCF	chr11:75863300-75863450	GM12865	blood:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
42	CTCF	chr11:75863320-75863470	GM12868	blood:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
43	CTCF	chr11:75863280-75863430	GM12873	blood:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
44	CTCF	chr11:75863259-75863522	ECC-1	luminal epithelium:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
45	CTCF	chr11:75863320-75863470	AG04449	skin:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
46	CTCF	chr11:75830240-75830390	HMEC	breast:	n/a	n/a
47	CTCF	chr11:75830100-75830250	A549	lung:	n/a	n/a
48	CTCF	chr11:75830260-75830410	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr11:75863300-75863450	GM12874	blood:	n/a	chr11:75863385-75863401 chr11:75863384-75863402
50	CTCF	chr11:75863320-75863470	NHEK	skin:	n/a	chr11:75863385-75863401 chr11:75863384-75863402

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75854042-75854092	AG09309	skin:	n/a
2	chr11:75852437-75852487	SK-N-SH	brain:	n/a
3	chr11:75852389-75852439	CMK	blood:	n/a
4	chr11:75852355-75852405	Hela-S3	cervix:	n/a
5	chr11:75831715-75831765	NHDF-neo	bronchial:	n/a
6	chr11:75831715-75831765	ovcar-3	ovarian:	n/a
7	chr11:75863429-75863479	HAEpiC	amniotic membrane:	n/a
8	chr11:75852389-75852439	HCT-116	colon:	n/a
9	chr11:75863429-75863479	T-47D	breast:	n/a
10	chr11:75863530-75863580	IMR90	lung:	fetal
11	chr11:75852437-75852487	HPAEpiC	pulmonary alveolar:	n/a
12	chr11:75863631-75863681	Jurkat	blood:	n/a
13	chr11:75831715-75831765	GM12892	blood:	n/a
14	chr11:75863631-75863681	MCF10A-Er-Src	breast:	n/a
15	chr11:75852437-75852487	SAEC	small airway:	n/a
16	chr11:75863429-75863479	HCT-116	colon:	n/a
17	chr11:75852437-75852487	AG04450	lung:	fetal
18	chr11:75863631-75863681	IMR90	lung:	fetal
19	chr11:75852355-75852405	NT2-D1	testis:	n/a
20	chr11:75854042-75854092	RPTEC	kidney:	n/a
21	chr11:75831715-75831765	GM12878	blood:	n/a
22	chr11:75863631-75863681	HL-60	blood:	n/a
23	chr11:75863631-75863681	GM12891	blood:	n/a
24	chr11:75854042-75854092	HMEC	breast:	n/a
25	chr11:75863429-75863479	HRE	kidney:	n/a
26	chr11:75852389-75852439	Hepatocyte	liver:	n/a
27	chr11:75852389-75852439	GM19239	blood:	n/a
28	chr11:75852389-75852439	PANC-1	pancreas:	n/a
29	chr11:75863429-75863479	H1-hESC	embryonic stem cell:	embryo
30	chr11:75863631-75863681	HRPEpiC	eye:	n/a
31	chr11:75863429-75863479	AG10803	skin:	n/a
32	chr11:75831715-75831765	PFSK-1	brain:	n/a
33	chr11:75863429-75863479	HRCEpiC	kidney:	n/a
34	chr11:75863631-75863681	AG04450	lung:	fetal
35	chr11:75863429-75863479	Hela-S3	cervix:	n/a
36	chr11:75831715-75831765	K562	blood:	n/a
37	chr11:75863530-75863580	HCF	heart:	n/a
38	chr11:75863429-75863479	HRPEpiC	eye:	n/a
39	chr11:75852355-75852405	HEK293	kidney:	embryo
40	chr11:75863429-75863479	HCM	heart:	n/a
41	chr11:75852355-75852405	HIPEpiC	eye:	n/a
42	chr11:75863631-75863681	HCF	heart:	n/a
43	chr11:75863429-75863479	NH-A	brain:	n/a
44	chr11:75863429-75863479	PrEC	prostate:	n/a
45	chr11:75852437-75852487	AG04449	skin:	fetal
46	chr11:75863631-75863681	SK-N-SH_RA	brain:	n/a
47	chr11:75852437-75852487	BE2_C	brain:	n/a
48	chr11:75854042-75854092	MCF10A-Er-Src	breast:	n/a
49	chr11:75863631-75863681	T-47D	breast:	n/a
50	chr11:75863530-75863580	NT2-D1	testis:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:75849232..75850781-chr11:75850823..75853731,2	K562	blood:
2	chr11:75840494..75842452-chr11:75842654..75844763,2	K562	blood:
3	chr11:75607077..75608544-chr11:75862937..75863839,5	K562	blood:
4	chr11:75864528..75867031-chr11:75871798..75873454,2	K562	blood:
5	chr11:75679377..75681059-chr11:75863070..75865584,2	MCF-7	breast:
6	chr11:75796883..75799472-chr11:75836520..75838163,2	K562	blood:
7	chr11:75841396..75843051-chr11:75844973..75846775,2	K562	blood:
8	chr11:75864698..75867155-chr11:75871013..75872936,2	MCF-7	breast:
9	chr11:75862929..75863882-chr11:76029395..76030079,4	K562	blood:
10	chr11:75634439..75636281-chr11:75851410..75853874,2	MCF-7	breast:
11	chr11:75858885..75860766-chr11:75865503..75867457,2	K562	blood:
12	chr11:75858885..75860766-chr11:75865503..75867457,2	K562	blood:
13	chr11:75823480..75825443-chr11:75829721..75831691,3	K562	blood:
14	chr11:75864249..75865220-chr11:76029478..76030050,2	MCF-7	breast:
15	chr11:75865596..75868388-chr11:75876534..75879243,2	K562	blood:
16	chr11:75817536..75821071-chr11:75829941..75832993,4	MCF-7	breast:
17	chr11:75818203..75819720-chr11:75822712..75825166,2	K562	blood:
18	chr11:75825744..75829389-chr11:75829480..75831593,3	K562	blood:
19	chr11:75822862..75824965-chr11:75825307..75828253,2	MCF-7	breast:
20	chr11:75817536..75821071-chr11:75829941..75832993,4	MCF-7	breast:
21	chr11:75829005..75831891-chr11:75836429..75839569,3	MCF-7	breast:
22	chr11:75849232..75850781-chr11:75850823..75853731,2	K562	blood:
23	chr11:75839101..75840628-chr11:75849802..75852307,2	MCF-7	breast:
24	chr11:75840494..75842452-chr11:75842654..75844763,2	K562	blood:
25	chr11:75848459..75850732-chr11:75852231..75854739,2	K562	blood:
26	chr11:75817741..75819762-chr11:75822475..75824409,2	MCF-7	breast:
27	chr11:75857248..75857816-chr11:76029548..76030103,2	K562	blood:
28	chr11:75839101..75840628-chr11:75849802..75852307,2	MCF-7	breast:
29	chr11:75829005..75831891-chr11:75836429..75839569,3	MCF-7	breast:
30	chr11:75848740..75850557-chr11:75852011..75854715,2	MCF-7	breast:
31	chr11:75848448..75850623-chr11:75852388..75854293,2	MCF-7	breast:
32	chr11:75823480..75825443-chr11:75829721..75831691,3	K562	blood:
33	chr11:75863959..75864459-chr7:152795919..152796557,2	MCF-7	breast:
34	chr11:75827427..75828061-chr11:75862929..75863644,2	MCF-7	breast:
35	chr11:75862934..75863810-chr11:75918354..75919268,2	K562	blood:
36	chr11:75840057..75843029-chr11:75846678..75850305,4	MCF-7	breast:
37	chr11:75841396..75843051-chr11:75844973..75846775,2	K562	blood:
38	chr11:75607743..75608566-chr11:75860272..75860889,2	K562	blood:
39	chr11:75607508..75608588-chr11:75862991..75863892,5	MCF-7	breast:
40	chr11:75827427..75828061-chr11:75862929..75863644,2	MCF-7	breast:
41	chr11:75855694..75857259-chr11:75861740..75864650,2	K562	blood:
42	chr11:75855694..75857259-chr11:75861740..75864650,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNT11-3	chr11:75830027-75830331	ucscGeneNc_uc009yui_1
2	lnc-WNT11-2	chr11:75848359-75848506	ENSG00000255421.1
3	lnc-WNT11-2	chr11:75848639-75848775	ENSG00000255421.1
4	lnc-WNT11-3	chr11:75832970-75833338	ucscGeneNc_uc009yui_1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UVRAG	hsa-miR-32-5p	chr11:75853509-75853515
2	UVRAG	hsa-miR-32-5p	chr11:75853494-75853516

Variant related genes	Relation type
UVRAG	TF binding region
ENSG00000255421	TF binding region
UVRAG	CpG island
ENSG00000255421	CpG island
ENSG00000198382	chromatin interactions
ENSG00000255421	chromatin interactions

Extended variants
information (count: 1762 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191865035	chr11:75820558-75820559	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183762405	chr11:75820563-75820564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568424920	chr11:75820576-75820577	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1521530	chr11:75820609-75820610	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs546915743	chr11:75820632-75820633	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188441026	chr11:75820647-75820648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538945680	chr11:75820651-75820652	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191465207	chr11:75820654-75820655	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7109676	chr11:75820691-75820692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77249863	chr11:75820695-75820696	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs55817225	chr11:75820729-75820730	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs373828505	chr11:75820732-75820733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554402389	chr11:75820749-75820750	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73498250	chr11:75820837-75820838	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539882659	chr11:75820901-75820902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76296602	chr11:75820969-75820970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376664886	chr11:75821007-75821008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146505029	chr11:75821011-75821012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74898911	chr11:75821067-75821068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562706954	chr11:75821069-75821070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185497194	chr11:75821115-75821116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542285715	chr11:75821147-75821148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562085565	chr11:75821148-75821149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190470399	chr11:75821191-75821192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181776392	chr11:75821207-75821208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112621687	chr11:75821247-75821248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547775958	chr11:75821249-75821250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10526191	chr11:75821255-75821256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35258205	chr11:75821256-75821257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61695799	chr11:75821275-75821276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139980959	chr11:75821354-75821355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368355191	chr11:75821394-75821395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76104320	chr11:75821443-75821444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552516770	chr11:75821454-75821455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569019188	chr11:75821458-75821459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537673264	chr11:75821649-75821650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74538954	chr11:75821664-75821665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78230097	chr11:75821675-75821676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115007439	chr11:75821676-75821677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553323374	chr11:75821751-75821752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576443420	chr11:75821781-75821782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185287677	chr11:75821783-75821784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539726542	chr11:75821787-75821788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556604550	chr11:75821788-75821789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528623088	chr11:75821796-75821797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188535144	chr11:75821813-75821814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149976783	chr11:75821908-75821909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542101807	chr11:75821916-75821917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376680162	chr11:75821953-75821954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145177710	chr11:75821971-75821972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75771800-75827000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:75779400-75827000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr11:75779800-75826600	Weak transcription	Fetal Thymus	thymus
4	chr11:75780400-75827000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:75785800-75827200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr11:75789000-75827200	Weak transcription	Liver	Liver
7	chr11:75789400-75846400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr11:75795000-75830000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr11:75798800-75827000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr11:75801200-75827000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr11:75801400-75826000	Weak transcription	Primary T cells from cord blood	blood
12	chr11:75801600-75826200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr11:75802000-75824200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr11:75802000-75826200	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr11:75802800-75834000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:75803400-75822200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:75808000-75827400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:75808400-75827000	Weak transcription	Placenta	Placenta
19	chr11:75812000-75826200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr11:75813600-75827000	Weak transcription	Spleen	Spleen
21	chr11:75814000-75825000	Weak transcription	K562	blood
22	chr11:75814000-75827000	Weak transcription	HUVEC	blood vessel
23	chr11:75814000-75830200	Weak transcription	Colon Smooth Muscle	Colon
24	chr11:75814200-75822400	Weak transcription	GM12878-XiMat	blood
25	chr11:75814200-75823000	Weak transcription	Fetal Muscle Leg	muscle
26	chr11:75814200-75823400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr11:75814200-75827000	Weak transcription	Left Ventricle	heart
28	chr11:75814200-75830200	Weak transcription	Right Ventricle	heart
29	chr11:75814400-75826400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr11:75814400-75826400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr11:75814400-75827000	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr11:75814400-75830800	Weak transcription	Ovary	ovary
33	chr11:75814400-75831000	Weak transcription	Fetal Heart	heart
34	chr11:75815800-75830400	Weak transcription	Fetal Brain Male	brain
35	chr11:75816000-75830800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:75817600-75821000	Strong transcription	Primary B cells from cord blood	blood
37	chr11:75818200-75827000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:75818400-75829800	Weak transcription	Stomach Smooth Muscle	stomach
39	chr11:75818600-75827000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:75818800-75823400	Strong transcription	Primary B cells from peripheral blood	blood
41	chr11:75819200-75820600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:75819400-75827000	Weak transcription	Fetal Stomach	stomach
43	chr11:75819400-75831600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:75819600-75820600	Enhancers	Brain Substantia Nigra	brain
45	chr11:75819600-75820800	Enhancers	NHDF-Ad	bronchial
46	chr11:75819600-75821000	Enhancers	Fetal Lung	lung
47	chr11:75819800-75820800	Enhancers	HepG2	liver
48	chr11:75819800-75827000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr11:75820200-75820800	Enhancers	Brain Anterior Caudate	brain
50	chr11:75820400-75820800	Enhancers	Brain Hippocampus Middle	brain

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