Variant report

Variant	nsv832112
Chromosome Location	chr11:33469782-33683052
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1685)
CpG islands
(count:1526)
Chromatin interactive
region (count:66)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33499524-33499864	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33529658-33529797	K562	blood:	n/a	n/a
3	ARID3A	chr11:33654861-33655278	HepG2	liver:	n/a	n/a
4	ATF1	chr11:33564551-33564917	K562	blood:	n/a	n/a
5	ATF2	chr11:33644267-33644768	GM12878	blood:	n/a	n/a
6	ATF2	chr11:33677655-33678205	GM12878	blood:	n/a	n/a
7	ATF2	chr11:33677704-33678167	GM12878	blood:	n/a	n/a
8	ATF2	chr11:33547216-33547636	GM12878	blood:	n/a	n/a
9	ATF3	chr11:33654730-33655484	A549	lung:	n/a	n/a
10	ATF3	chr11:33654742-33655408	A549	lung:	n/a	n/a
11	BACH1	chr11:33654944-33655263	H1-hESC	embryonic stem cell:	n/a	chr11:33655157-33655171
12	BACH1	chr11:33639584-33639906	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:33682557-33682825	GM12878	blood:	n/a	n/a
14	BATF	chr11:33677732-33678086	GM12878	blood:	n/a	n/a
15	BATF	chr11:33547665-33547985	GM12878	blood:	n/a	n/a
16	BATF	chr11:33596965-33597171	GM12878	blood:	n/a	n/a
17	BATF	chr11:33656060-33656384	GM12878	blood:	n/a	n/a
18	BATF	chr11:33547673-33547858	GM12878	blood:	n/a	n/a
19	BATF	chr11:33643824-33644101	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:33677762-33678140	GM12878	blood:	n/a	n/a
21	BCL11A	chr11:33677847-33678082	GM12878	blood:	n/a	n/a
22	BCL3	chr11:33547150-33547634	GM12878	blood:	n/a	n/a
23	BCL3	chr11:33655856-33656477	A549	lung:	n/a	n/a
24	BCL3	chr11:33655767-33656461	A549	lung:	n/a	n/a
25	BCL3	chr11:33677762-33678111	GM12878	blood:	n/a	n/a
26	BCL3	chr11:33654667-33655278	A549	lung:	n/a	n/a
27	BCL3	chr11:33512690-33512977	GM12878	blood:	n/a	n/a
28	BCL3	chr11:33654661-33655470	A549	lung:	n/a	n/a
29	BCLAF1	chr11:33677662-33678238	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:33529628-33529796	K562	blood:	n/a	n/a
31	BHLHE40	chr11:33672182-33672413	HepG2	liver:	n/a	n/a
32	BHLHE40	chr11:33484666-33484886	K562	blood:	n/a	n/a
33	BHLHE40	chr11:33654722-33655370	HepG2	liver:	n/a	n/a
34	BRCA1	chr11:33654876-33655052	HepG2	liver:	n/a	n/a
35	CBX3	chr11:33654718-33655684	HCT-116	colon:	n/a	n/a
36	CBX3	chr11:33654705-33655641	HCT-116	colon:	n/a	n/a
37	CCNT2	chr11:33544760-33544923	K562	blood:	n/a	n/a
38	CEBPB	chr11:33529486-33529976	K562	blood:	n/a	chr11:33529678-33529689
39	CEBPB	chr11:33656742-33657148	A549	lung:	n/a	chr11:33656939-33656952 chr11:33656941-33656952 chr11:33656939-33656950
40	CEBPB	chr11:33657585-33658156	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:33499621-33499855	HepG2	liver:	n/a	chr11:33499751-33499762
42	CEBPB	chr11:33607146-33607488	A549	lung:	n/a	chr11:33607270-33607281 chr11:33607269-33607282
43	CEBPB	chr11:33483885-33484074	HepG2	liver:	n/a	chr11:33483952-33483963
44	CEBPB	chr11:33674500-33674813	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:33609812-33610126	IMR90	lung:	n/a	chr11:33609983-33609996
46	CEBPB	chr11:33529362-33530034	HCT-116	colon:	n/a	chr11:33529678-33529689
47	CEBPB	chr11:33655772-33656554	HCT-116	colon:	n/a	n/a
48	CEBPB	chr11:33474376-33474661	IMR90	lung:	n/a	n/a
49	CEBPB	chr11:33499567-33499966	MCF-7	breast:	n/a	chr11:33499751-33499762
50	CEBPB	chr11:33532926-33533229	HepG2	liver:	n/a	chr11:33533070-33533081 chr11:33533079-33533091

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33680427-33680477	T-47D	breast:	n/a
2	chr11:33680427-33680477	T-47D	breast:	n/a
3	chr11:33680332-33680382	HCF	heart:	n/a
4	chr11:33562503-33562553	K562	blood:	n/a
5	chr11:33677621-33677671	IMR90	lung:	fetal
6	chr11:33680427-33680477	AG04449	skin:	fetal
7	chr11:33680220-33680270	LNCaP	prostate:	n/a
8	chr11:33563377-33563427	CMK	blood:	n/a
9	chr11:33680427-33680477	ECC-1	luminal epithelium:	n/a
10	chr11:33640167-33640217	HRCEpiC	kidney:	n/a
11	chr11:33474484-33474534	HL-60	blood:	n/a
12	chr11:33677621-33677671	SK-N-SH	brain:	n/a
13	chr11:33563946-33563996	GM19239	blood:	n/a
14	chr11:33680220-33680270	SKMC	muscle:	n/a
15	chr11:33673943-33673993	HUVEC	blood vessel:	n/a
16	chr11:33563060-33563110	GM06990	blood:	n/a
17	chr11:33682676-33682726	H1-hESC	embryonic stem cell:	embryo
18	chr11:33563060-33563110	NHBE	bronchial:	n/a
19	chr11:33667433-33667483	SK-N-SH_RA	brain:	n/a
20	chr11:33682676-33682726	SK-N-SH_RA	brain:	n/a
21	chr11:33563060-33563110	Jurkat	blood:	n/a
22	chr11:33667433-33667483	NB4	blood:	n/a
23	chr11:33652171-33652221	ECC-1	luminal epithelium:	n/a
24	chr11:33563720-33563770	GM12878	blood:	n/a
25	chr11:33474484-33474534	PrEC	prostate:	n/a
26	chr11:33563377-33563427	HCPEpiC	choroid plexus:	n/a
27	chr11:33637874-33637924	GM12892	blood:	n/a
28	chr11:33474484-33474534	AG04449	skin:	fetal
29	chr11:33677621-33677671	ECC-1	luminal epithelium:	n/a
30	chr11:33680273-33680323	GM12891	blood:	n/a
31	chr11:33563720-33563770	ECC-1	luminal epithelium:	n/a
32	chr11:33652171-33652221	PrEC	prostate:	n/a
33	chr11:33562503-33562553	HCT-116	colon:	n/a
34	chr11:33474484-33474534	GM12892	blood:	n/a
35	chr11:33640167-33640217	MCF-7	breast:	n/a
36	chr11:33563377-33563427	T-47D	breast:	n/a
37	chr11:33563946-33563996	A549	lung:	n/a
38	chr11:33656146-33656196	HCT-116	colon:	n/a
39	chr11:33680427-33680477	HEK293	kidney:	embryo
40	chr11:33554009-33554059	PrEC	prostate:	n/a
41	chr11:33554009-33554059	HIPEpiC	eye:	n/a
42	chr11:33554009-33554059	GM12891	blood:	n/a
43	chr11:33563946-33563996	PFSK-1	brain:	n/a
44	chr11:33563946-33563996	GM12878	blood:	n/a
45	chr11:33563720-33563770	A549	lung:	n/a
46	chr11:33679728-33679778	AoSMC	blood vessel:	n/a
47	chr11:33677621-33677671	Hepatocyte	liver:	n/a
48	chr11:33681423-33681473	NHDF-neo	bronchial:	n/a
49	chr11:33563377-33563427	BE2_C	brain:	n/a
50	chr11:33562503-33562553	H1-hESC	embryonic stem cell:	embryo

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:33530740..33532522-chr11:33535502..33537304,2	MCF-7	breast:
2	chr11:33579969..33581756-chr11:33591394..33593164,2	K562	blood:
3	chr11:33674641..33678001-chr11:33680305..33683108,3	K562	blood:
4	chr11:33513897..33516124-chr11:33565308..33567092,2	K562	blood:
5	chr11:33639712..33641762-chr11:33643100..33644997,2	K562	blood:
6	chr11:33492401..33495030-chr11:33579028..33581044,2	K562	blood:
7	chr11:33654474..33658649-chr11:33659750..33663424,5	MCF-7	breast:
8	chr11:33517532..33520480-chr11:33524551..33527358,2	K562	blood:
9	chr11:33596599..33600481-chr11:33606542..33609139,3	K562	blood:
10	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
11	chr11:33530740..33532522-chr11:33535502..33537304,2	MCF-7	breast:
12	chr11:33564209..33565238-chr11:33709135..33709867,4	MCF-7	breast:
13	chr11:33518367..33520267-chr11:33520431..33522764,2	K562	blood:
14	chr11:33596418..33599960-chr11:33602202..33605438,3	K562	blood:
15	chr11:33587229..33589427-chr11:33594919..33597666,2	MCF-7	breast:
16	chr11:33654474..33658649-chr11:33659750..33663424,5	MCF-7	breast:
17	chr11:33534524..33537058-chr11:33559192..33562148,2	K562	blood:
18	chr11:33596418..33599960-chr11:33602202..33605438,3	K562	blood:
19	chr11:33593866..33595976-chr11:33607119..33609770,2	K562	blood:
20	chr11:33651094..33655040-chr11:33655885..33660180,5	MCF-7	breast:
21	chr11:33497434..33499618-chr11:33502949..33504703,2	K562	blood:
22	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
23	chr11:33513897..33516124-chr11:33565308..33567092,2	K562	blood:
24	chr11:33596599..33600481-chr11:33606542..33609139,3	K562	blood:
25	chr11:33530109..33532353-chr11:33535531..33537210,2	K562	blood:
26	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
27	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
28	chr11:33639712..33641762-chr11:33643100..33644997,2	K562	blood:
29	chr11:33587229..33589427-chr11:33594919..33597666,2	MCF-7	breast:
30	chr11:33564733..33567080-chr11:33738231..33740368,2	K562	blood:
31	chr11:33530109..33532353-chr11:33535531..33537210,2	K562	blood:
32	chr11:33603962..33604462-chr6:27804423..27805235,2	HCT-116	colon:
33	chr11:33614618..33616551-chr11:33617478..33619147,2	K562	blood:
34	chr11:33492401..33495030-chr11:33579028..33581044,2	K562	blood:
35	chr11:33548771..33550740-chr11:33552421..33555273,2	K562	blood:
36	chr11:33497434..33499618-chr11:33502949..33504703,2	K562	blood:
37	chr11:33667138..33667889-chr11:33850774..33851566,2	K562	blood:
38	chr11:33616152..33618117-chr11:33620573..33622501,2	K562	blood:
39	chr11:33602299..33604468-chr11:33607477..33609270,2	K562	blood:
40	chr11:33548771..33550740-chr11:33552421..33555273,2	K562	blood:
41	chr11:33534524..33537058-chr11:33559192..33562148,2	K562	blood:
42	chr11:33564210..33565457-chr11:33703688..33704553,5	MCF-7	breast:
43	chr11:33602299..33604468-chr11:33607477..33609270,2	K562	blood:
44	chr11:33565766..33566276-chr11:33851021..33851593,2	K562	blood:
45	chr11:33614618..33616551-chr11:33617478..33619147,2	K562	blood:
46	chr11:33582088..33585071-chr11:33604919..33607475,2	MCF-7	breast:
47	chr11:33674641..33678001-chr11:33680305..33683108,3	K562	blood:
48	chr11:33564143..33565156-chr11:33703966..33705027,5	MCF-7	breast:
49	chr11:32450252..32452924-chr11:33665235..33667527,2	K562	blood:
50	chr11:33517532..33520401-chr11:33525287..33527358,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD59-1	chr11:33676827-33676991	NONHSAT018702
2	lnc-CD59-4	chr11:33677663-33677742	ucscGeneNc_uc001muq_1
3	lnc-CD59-1	chr11:33675753-33676577	NONHSAT018702
4	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701
5	lnc-CD59-1	chr11:33676877-33676991	NONHSAT018703
6	lnc-CD59-4	chr11:33676579-33676636	ucscGeneNc_uc001muq_1
7	lnc-CD59-4	chr11:33678367-33678519	ucscGeneNc_uc001muq_1

No data

Variant related genes	Relation type
ENSG00000255207	TF binding region
KIAA1549L	TF binding region
ENSG00000255207	CpG island
KIAA1549L	CpG island
ENSG00000255207	chromatin interactions
ENSG00000184937	chromatin interactions

Extended variants
information (count: 7911 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:7911 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2761222	chr11:33469808-33469809	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs557930102	chr11:33469852-33469853	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs546111209	chr11:33469875-33469876	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs2761221	chr11:33469880-33469881	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs576143176	chr11:33469894-33469895	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544971960	chr11:33470125-33470126	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs368468534	chr11:33470130-33470131	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs573408290	chr11:33470141-33470142	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558532022	chr11:33470186-33470187	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201930949	chr11:33470203-33470204	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs541399206	chr11:33470206-33470207	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187587261	chr11:33470211-33470212	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs530256724	chr11:33470212-33470213	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs189921710	chr11:33470216-33470217	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs562543043	chr11:33470217-33470218	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576088932	chr11:33470237-33470238	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs4756696	chr11:33470268-33470269	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs551357403	chr11:33470279-33470280	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs139642509	chr11:33470324-33470325	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs527580852	chr11:33470356-33470357	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs76744874	chr11:33470376-33470377	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567440357	chr11:33470389-33470390	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561596099	chr11:33470395-33470396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs536024368	chr11:33470445-33470446	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs12272604	chr11:33470454-33470455	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs16924336	chr11:33470473-33470474	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs77478311	chr11:33470515-33470516	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs558517099	chr11:33470573-33470574	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572392577	chr11:33470582-33470583	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs541687961	chr11:33470601-33470602	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs181593132	chr11:33470668-33470669	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs575100004	chr11:33470723-33470724	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs543987786	chr11:33470764-33470765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563884440	chr11:33470773-33470774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553540920	chr11:33470780-33470781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79831408	chr11:33470791-33470792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75457615	chr11:33470792-33470793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545171603	chr11:33470823-33470824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542009810	chr11:33470879-33470880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185360481	chr11:33470947-33470948	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs527323529	chr11:33470977-33470978	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs116414810	chr11:33470987-33470988	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs149753375	chr11:33471043-33471044	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs190119634	chr11:33471168-33471169	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs142792786	chr11:33471231-33471232	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs182074435	chr11:33471255-33471256	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs7951843	chr11:33471306-33471307	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs76914189	chr11:33471350-33471351	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145183708	chr11:33471425-33471426	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs74784027	chr11:33471442-33471443	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33466600-33471000	Weak transcription	Brain Anterior Caudate	brain
2	chr11:33466800-33474400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:33467200-33480200	Weak transcription	Fetal Brain Female	brain
4	chr11:33467400-33469800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:33467400-33470200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:33467400-33471000	Weak transcription	A549	lung
7	chr11:33467400-33474200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:33467400-33474200	Weak transcription	NHLF	lung
9	chr11:33467600-33470400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:33467600-33471000	Weak transcription	NHDF-Ad	bronchial
11	chr11:33467600-33474200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:33467800-33471000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:33468200-33469800	Weak transcription	HUVEC	blood vessel
14	chr11:33468200-33470200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr11:33468400-33469800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr11:33468400-33473400	Weak transcription	HSMMtube	muscle
17	chr11:33468600-33469800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:33468600-33469800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:33468600-33469800	Weak transcription	Osteobl	bone
20	chr11:33468600-33474200	Weak transcription	HSMM	muscle
21	chr11:33468800-33469800	Weak transcription	NH-A	brain
22	chr11:33468800-33471000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:33469200-33471400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr11:33469800-33471200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:33469800-33471400	Enhancers	HUVEC	blood vessel
26	chr11:33469800-33471600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:33469800-33471600	Enhancers	Osteobl	bone
28	chr11:33469800-33472000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:33469800-33472000	Enhancers	NH-A	brain
30	chr11:33469800-33472200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:33470000-33471200	Enhancers	HMEC	breast
32	chr11:33470200-33470400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:33470200-33471600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr11:33470400-33470800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:33470400-33472000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:33470800-33472600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr11:33471000-33471200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:33471000-33471200	Enhancers	Brain Anterior Caudate	brain
39	chr11:33471000-33471200	Enhancers	A549	lung
40	chr11:33471000-33471400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr11:33471000-33471400	Enhancers	NHDF-Ad	bronchial
42	chr11:33471000-33471800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:33471200-33471600	Flanking Active TSS	A549	lung
44	chr11:33471200-33471800	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr11:33471200-33474200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:33471200-33474200	Weak transcription	HMEC	breast
47	chr11:33471400-33473600	Weak transcription	HUVEC	blood vessel
48	chr11:33471400-33474200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:33471400-33474200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:33471400-33474200	Weak transcription	NHDF-Ad	bronchial

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