Variant report

Variant	nsv553996
Chromosome Location	chr11:33383085-33540676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1226)
CpG islands
(count:1039)
Chromatin interactive
region (count:67)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33529658-33529797	K562	blood:	n/a	n/a
2	ARID3A	chr11:33394101-33394301	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:33383912-33384198	K562	blood:	n/a	n/a
4	ARID3A	chr11:33499524-33499864	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:33383925-33384254	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
7	ATF1	chr11:33394198-33394335	K562	blood:	n/a	n/a
8	ATF2	chr11:33404542-33405049	GM12878	blood:	n/a	n/a
9	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
10	ATF2	chr11:33404441-33405009	GM12878	blood:	n/a	n/a
11	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
12	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
13	BACH1	chr11:33397385-33398563	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr11:33404521-33404947	GM12878	blood:	n/a	n/a
15	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a
16	BATF	chr11:33404575-33404911	GM12878	blood:	n/a	n/a
17	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
18	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:33409556-33409888	GM12878	blood:	n/a	n/a
20	BCL11A	chr11:33409572-33409836	GM12878	blood:	n/a	n/a
21	BCL11A	chr11:33409034-33409543	GM12878	blood:	n/a	n/a
22	BCL11A	chr11:33404557-33404945	GM12878	blood:	n/a	n/a
23	BCL3	chr11:33404619-33404913	GM12878	blood:	n/a	n/a
24	BCL3	chr11:33512690-33512977	GM12878	blood:	n/a	n/a
25	BCL3	chr11:33409282-33409904	GM12878	blood:	n/a	n/a
26	BCLAF1	chr11:33404519-33404990	GM12878	blood:	n/a	n/a
27	BCLAF1	chr11:33409067-33410001	GM12878	blood:	n/a	n/a
28	BCLAF1	chr11:33409061-33410037	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:33427892-33427983	K562	blood:	n/a	n/a
30	BHLHE40	chr11:33484666-33484886	K562	blood:	n/a	n/a
31	BHLHE40	chr11:33404539-33405771	GM12878	blood:	n/a	n/a
32	BHLHE40	chr11:33401529-33401825	GM12878	blood:	n/a	n/a
33	BHLHE40	chr11:33529628-33529796	K562	blood:	n/a	n/a
34	CEBPB	chr11:33488148-33488342	A549	lung:	n/a	n/a
35	CEBPB	chr11:33425244-33425411	IMR90	lung:	n/a	n/a
36	CEBPB	chr11:33468747-33468988	IMR90	lung:	n/a	chr11:33468877-33468890 chr11:33468878-33468889
37	CEBPB	chr11:33529381-33529988	MCF-7	breast:	n/a	chr11:33529678-33529689
38	CEBPB	chr11:33529449-33529916	ECC-1	luminal epithelium:	n/a	chr11:33529678-33529689
39	CEBPB	chr11:33529536-33529876	K562	blood:	n/a	chr11:33529678-33529689
40	CEBPB	chr11:33532945-33533237	A549	lung:	n/a	chr11:33533070-33533081 chr11:33533079-33533091
41	CEBPB	chr11:33529426-33529916	K562	blood:	n/a	chr11:33529678-33529689
42	CEBPB	chr11:33512741-33512973	HepG2	liver:	n/a	chr11:33512889-33512900
43	CEBPB	chr11:33499578-33499951	HepG2	liver:	n/a	chr11:33499751-33499762
44	CEBPB	chr11:33529283-33530043	HCT-116	colon:	n/a	chr11:33529678-33529689
45	CEBPB	chr11:33499570-33499963	HepG2	liver:	n/a	chr11:33499751-33499762
46	CEBPB	chr11:33499528-33499927	HepG2	liver:	n/a	chr11:33499751-33499762
47	CEBPB	chr11:33417928-33418277	IMR90	lung:	n/a	chr11:33418096-33418109 chr11:33418098-33418107 chr11:33418096-33418107 chr11:33418098-33418107 chr11:33418098-33418107
48	CEBPB	chr11:33529285-33530058	MCF-7	breast:	n/a	chr11:33529678-33529689
49	CEBPB	chr11:33537039-33537406	IMR90	lung:	n/a	n/a
50	CEBPB	chr11:33532999-33533115	Hela-S3	cervix:	n/a	chr11:33533070-33533081 chr11:33533079-33533091

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33397153-33397203	GM06990	blood:	n/a
2	chr11:33397679-33397729	AG04449	skin:	fetal
3	chr11:33397153-33397203	GM06990	blood:	n/a
4	chr11:33397679-33397729	AG04449	skin:	fetal
5	chr11:33397689-33397739	K562	blood:	n/a
6	chr11:33397679-33397729	Hela-S3	cervix:	n/a
7	chr11:33396983-33397033	MCF10A-Er-Src	breast:	n/a
8	chr11:33399978-33400028	Hepatocyte	liver:	n/a
9	chr11:33453389-33453439	HMEC	breast:	n/a
10	chr11:33399978-33400028	HMEC	breast:	n/a
11	chr11:33399978-33400028	NB4	blood:	n/a
12	chr11:33397387-33397437	Caco-2	colon:	n/a
13	chr11:33474484-33474534	LNCaP	prostate:	n/a
14	chr11:33397153-33397203	H1-hESC	embryonic stem cell:	embryo
15	chr11:33398366-33398416	GM12892	blood:	n/a
16	chr11:33398245-33398295	ProgFib	skin:	n/a
17	chr11:33400574-33400624	MCF-7	breast:	n/a
18	chr11:33394273-33394323	H1-hESC	embryonic stem cell:	embryo
19	chr11:33399978-33400028	NT2-D1	testis:	n/a
20	chr11:33453389-33453439	K562	blood:	n/a
21	chr11:33398366-33398416	NT2-D1	testis:	n/a
22	chr11:33474484-33474534	Hepatocyte	liver:	n/a
23	chr11:33396983-33397033	PrEC	prostate:	n/a
24	chr11:33398173-33398223	PrEC	prostate:	n/a
25	chr11:33400574-33400624	HEEpiC	esophagus:	n/a
26	chr11:33398245-33398295	PFSK-1	brain:	n/a
27	chr11:33397153-33397203	ProgFib	skin:	n/a
28	chr11:33453389-33453439	HepG2	liver:	n/a
29	chr11:33397387-33397437	LNCaP	prostate:	n/a
30	chr11:33397387-33397437	A549	lung:	n/a
31	chr11:33398366-33398416	AG09319	gingival:	n/a
32	chr11:33397679-33397729	PANC-1	pancreas:	n/a
33	chr11:33400574-33400624	PFSK-1	brain:	n/a
34	chr11:33397689-33397739	A549	lung:	n/a
35	chr11:33397387-33397437	HRE	kidney:	n/a
36	chr11:33396983-33397033	ProgFib	skin:	n/a
37	chr11:33397679-33397729	HEEpiC	esophagus:	n/a
38	chr11:33397387-33397437	PANC-1	pancreas:	n/a
39	chr11:33399978-33400028	AoSMC	blood vessel:	n/a
40	chr11:33396859-33396909	HCPEpiC	choroid plexus:	n/a
41	chr11:33397821-33397871	HRPEpiC	eye:	n/a
42	chr11:33397689-33397739	AG09319	gingival:	n/a
43	chr11:33397689-33397739	SK-N-MC	brain:	n/a
44	chr11:33398173-33398223	GM12891	blood:	n/a
45	chr11:33506184-33506234	HL-60	blood:	n/a
46	chr11:33397821-33397871	HEEpiC	esophagus:	n/a
47	chr11:33474484-33474534	ProgFib	skin:	n/a
48	chr11:33396859-33396909	SKMC	muscle:	n/a
49	chr11:33400574-33400624	LNCaP	prostate:	n/a
50	chr11:33397153-33397203	NHDF-neo	bronchial:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:33383304..33384229-chr11:33708679..33709748,3	MCF-7	breast:
2	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
3	chr11:33391648..33394205-chr11:33396367..33400084,3	K562	blood:
4	chr11:33530109..33532353-chr11:33535531..33537210,2	K562	blood:
5	chr11:33416676..33419367-chr11:33423190..33425357,2	K562	blood:
6	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
7	chr11:32982327..32984023-chr11:33390393..33392493,2	K562	blood:
8	chr11:33518367..33520267-chr11:33520431..33522764,2	K562	blood:
9	chr11:33412811..33414591-chr11:33744029..33746622,2	K562	blood:
10	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
11	chr11:33383578..33384538-chr11:33708929..33709708,5	K562	blood:
12	chr11:33403805..33405903-chr11:33414463..33417062,2	MCF-7	breast:
13	chr11:33530740..33532522-chr11:33535502..33537304,2	MCF-7	breast:
14	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
15	chr11:33396319..33398155-chr11:33401081..33403706,2	MCF-7	breast:
16	chr11:33419522..33421501-chr11:33424149..33426108,2	K562	blood:
17	chr11:33384382..33386417-chr11:33393888..33396516,2	K562	blood:
18	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
19	chr11:33395838..33399105-chr11:33400150..33402846,3	MCF-7	breast:
20	chr11:33403805..33405903-chr11:33414463..33417062,2	MCF-7	breast:
21	chr11:33534524..33537058-chr11:33559192..33562148,2	K562	blood:
22	chr11:33492401..33495030-chr11:33579028..33581044,2	K562	blood:
23	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
24	chr11:33187508..33188019-chr11:33392733..33393351,2	MCF-7	breast:
25	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
26	chr11:33392077..33394205-chr11:33397342..33400084,3	K562	blood:
27	chr11:33517532..33520480-chr11:33524551..33527358,2	K562	blood:
28	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
29	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
30	chr11:33428202..33430119-chr11:33432481..33434506,2	MCF-7	breast:
31	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
32	chr11:33351340..33351943-chr11:33383658..33384527,2	K562	blood:
33	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
34	chr11:33422636..33425023-chr11:33427111..33429775,2	MCF-7	breast:
35	chr11:33497434..33499618-chr11:33502949..33504703,2	K562	blood:
36	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
37	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
38	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
39	chr11:33474719..33477394-chr11:33482084..33484055,2	K562	blood:
40	chr11:33380757..33382861-chr11:33395684..33398398,2	MCF-7	breast:
41	chr11:33530740..33532522-chr11:33535502..33537304,2	MCF-7	breast:
42	chr11:33517532..33520480-chr11:33524551..33527358,2	K562	blood:
43	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
44	chr11:33179272..33181255-chr11:33382560..33384208,2	K562	blood:
45	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
46	chr11:33399022..33400859-chr11:33402110..33404984,2	K562	blood:
47	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
48	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
49	chr11:33530109..33532353-chr11:33535531..33537210,2	K562	blood:
50	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700
2	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701

No data

Variant related genes	Relation type
ENSG00000255207	TF binding region
ENSG00000254537	TF binding region
ENSG00000255207	CpG island
ENSG00000254537	CpG island
ENSG00000254537	chromatin interactions
ENSG00000255207	chromatin interactions
ENSG00000085063	chromatin interactions

Extended variants
information (count: 5701 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:5701 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3847595	chr11:33383085-33383086	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549308430	chr11:33383091-33383092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569436864	chr11:33383125-33383126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536705511	chr11:33383161-33383162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143379521	chr11:33383164-33383165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185313289	chr11:33383176-33383177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77444834	chr11:33383218-33383219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553036274	chr11:33383255-33383256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566760766	chr11:33383256-33383257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535798785	chr11:33383328-33383329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555227363	chr11:33383335-33383336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3908395	chr11:33383339-33383340	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544346840	chr11:33383441-33383442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558255525	chr11:33383444-33383445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs16924228	chr11:33383448-33383449	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs79298452	chr11:33383473-33383474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560154778	chr11:33383494-33383495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529497266	chr11:33383619-33383620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11032236	chr11:33383648-33383649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562905134	chr11:33383695-33383696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531952174	chr11:33383722-33383723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78556924	chr11:33383752-33383753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190861892	chr11:33383787-33383788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570544545	chr11:33383794-33383795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533098070	chr11:33383818-33383819	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs199544098	chr11:33383886-33383887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs376992654	chr11:33383899-33383900	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs184025097	chr11:33383910-33383911	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566480715	chr11:33383931-33383932	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs535709710	chr11:33383937-33383938	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs568674665	chr11:33384032-33384033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11605664	chr11:33384046-33384047	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs538023889	chr11:33384077-33384078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34744717	chr11:33384103-33384104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557702840	chr11:33384118-33384119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577707003	chr11:33384119-33384120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111328943	chr11:33384138-33384139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553833158	chr11:33384151-33384152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370158088	chr11:33384153-33384154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374749530	chr11:33384195-33384196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187424490	chr11:33384230-33384231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573712276	chr11:33384258-33384259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142718588	chr11:33384302-33384303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563173391	chr11:33384304-33384305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367870981	chr11:33384328-33384329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs151243684	chr11:33384330-33384331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565523980	chr11:33384350-33384351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533014710	chr11:33384356-33384357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553477460	chr11:33384416-33384417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546730194	chr11:33384419-33384420	Weak transcription	n/a	n/a	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	18451855	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

Chromatin state (count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33369600-33383800	Weak transcription	Stomach Mucosa	stomach
2	chr11:33372000-33392400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:33372200-33383600	Weak transcription	Small Intestine	intestine
4	chr11:33373800-33383600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr11:33375200-33383600	Weak transcription	Hela-S3	cervix
6	chr11:33375200-33392600	Weak transcription	Pancreas	Pancrea
7	chr11:33375400-33383600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:33375400-33383800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr11:33375400-33383800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr11:33375600-33383600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr11:33375600-33383800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr11:33375600-33383800	Weak transcription	Thymus	Thymus
13	chr11:33375800-33383600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr11:33375800-33383800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr11:33375800-33383800	Weak transcription	Brain Anterior Caudate	brain
16	chr11:33375800-33383800	Weak transcription	Colon Smooth Muscle	Colon
17	chr11:33375800-33383800	Weak transcription	Fetal Thymus	thymus
18	chr11:33375800-33388400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:33376000-33383600	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr11:33376000-33383600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr11:33376000-33383600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr11:33376000-33383600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr11:33376000-33383600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:33376000-33383600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:33376000-33383600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr11:33376000-33383600	Weak transcription	HMEC	breast
27	chr11:33376000-33383800	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr11:33376200-33383600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:33376200-33383600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr11:33376200-33383600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr11:33376200-33383800	Weak transcription	Rectal Smooth Muscle	rectum
32	chr11:33376200-33383800	Weak transcription	HSMMtube	muscle
33	chr11:33376200-33386400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr11:33376400-33383600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:33376400-33383600	Weak transcription	NHDF-Ad	bronchial
36	chr11:33376600-33383600	Weak transcription	Osteobl	bone
37	chr11:33376600-33383800	Weak transcription	Adipose Nuclei	Adipose
38	chr11:33376800-33383600	Weak transcription	A549	lung
39	chr11:33376800-33383800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr11:33376800-33390800	Weak transcription	NH-A	brain
41	chr11:33377200-33383200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr11:33377200-33383600	Weak transcription	Dnd41	blood
43	chr11:33377200-33383800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr11:33377600-33383600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:33377600-33383800	Weak transcription	Liver	Liver
46	chr11:33378600-33383600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:33378800-33383800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:33379000-33383600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:33379000-33383600	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr11:33379000-33383800	Weak transcription	Monocytes-CD14+_RO01746	blood

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