Variant report

Variant	nsv832172
Chromosome Location	chr11:59396407-59431115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59425594-59425707	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:59410927-59411247	HepG2	liver:	n/a	n/a
3	ATF1	chr11:59415189-59415389	K562	blood:	n/a	n/a
4	BHLHE40	chr11:59415178-59415394	K562	blood:	n/a	n/a
5	CEBPB	chr11:59418917-59419127	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:59425618-59425812	Hela-S3	cervix:	n/a	chr11:59425672-59425683
7	CEBPB	chr11:59410835-59411375	A549	lung:	n/a	chr11:59411115-59411126
8	CEBPB	chr11:59425606-59425806	H1-hESC	embryonic stem cell:	n/a	chr11:59425672-59425683
9	CEBPB	chr11:59410936-59411298	Hela-S3	cervix:	n/a	chr11:59411115-59411126
10	CEBPB	chr11:59410996-59411194	HepG2	liver:	n/a	chr11:59411115-59411126
11	CEBPB	chr11:59410968-59411199	MCF-7	breast:	n/a	chr11:59411115-59411126
12	CEBPB	chr11:59425580-59425872	HepG2	liver:	n/a	chr11:59425672-59425683
13	CEBPB	chr11:59410946-59411272	IMR90	lung:	n/a	chr11:59411115-59411126
14	CEBPB	chr11:59410927-59411301	HepG2	liver:	n/a	chr11:59411115-59411126
15	CEBPB	chr11:59410924-59411317	HepG2	liver:	n/a	chr11:59411115-59411126
16	CEBPB	chr11:59410956-59411263	HepG2	liver:	n/a	chr11:59411115-59411126
17	CEBPB	chr11:59410944-59411277	A549	lung:	n/a	chr11:59411115-59411126
18	CEBPB	chr11:59410933-59411286	K562	blood:	n/a	chr11:59411115-59411126
19	CEBPD	chr11:59410948-59411198	HepG2	liver:	n/a	n/a
20	CEBPD	chr11:59410919-59411246	HepG2	liver:	n/a	n/a
21	CTCF	chr11:59399615-59399642	Fibrobl	skin:	n/a	n/a
22	CTCF	chr11:59410500-59410650	HEK293	kidney:	n/a	chr11:59410564-59410573
23	CTCF	chr11:59426854-59426875	GM13976	blood:	n/a	n/a
24	EP300	chr11:59410942-59411251	HepG2	liver:	n/a	chr11:59411224-59411238
25	EP300	chr11:59415113-59415367	K562	blood:	n/a	n/a
26	FAM48A	chr11:59410924-59411051	GM12878	blood:	n/a	n/a
27	FOS	chr11:59408810-59408841	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr11:59408731-59408917	MCF10A-Er-Src	breast:	n/a	chr11:59408839-59408848 chr11:59408839-59408846 chr11:59408838-59408847 chr11:59408839-59408847 chr11:59408837-59408849
29	FOS	chr11:59408716-59408901	MCF10A-Er-Src	breast:	n/a	chr11:59408839-59408848 chr11:59408839-59408846 chr11:59408838-59408847 chr11:59408839-59408847 chr11:59408837-59408849
30	FOXA1	chr11:59410840-59411288	HepG2	liver:	n/a	n/a
31	FOXA2	chr11:59410900-59411173	HepG2	liver:	n/a	n/a
32	GATA2	chr11:59428155-59428557	SH-SY5Y	brain:	n/a	chr11:59428291-59428302
33	GATA3	chr11:59429627-59430120	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr11:59418321-59418444	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr11:59416374-59416530	SH-SY5Y	brain:	n/a	n/a
36	HNF4A	chr11:59410953-59411213	HepG2	liver:	n/a	n/a
37	HNF4A	chr11:59410873-59411297	HepG2	liver:	n/a	n/a
38	HNF4G	chr11:59410932-59411224	HepG2	liver:	n/a	n/a
39	JUN	chr11:59408828-59408939	HepG2	liver:	n/a	chr11:59408839-59408848 chr11:59408839-59408846 chr11:59408838-59408847 chr11:59408839-59408847 chr11:59408837-59408849
40	JUN	chr11:59428160-59428290	K562	blood:	n/a	n/a
41	JUN	chr11:59425665-59425738	HepG2	liver:	n/a	chr11:59425673-59425686
42	JUN	chr11:59415188-59415343	K562	blood:	n/a	n/a
43	JUN	chr11:59418098-59418209	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr11:59425590-59425783	HepG2	liver:	n/a	n/a
45	JUND	chr11:59408470-59409106	SK-N-SH	brain:	n/a	chr11:59408837-59408848 chr11:59408839-59408848 chr11:59408839-59408846 chr11:59408838-59408847 chr11:59408839-59408847 chr11:59408837-59408849
46	JUND	chr11:59408669-59408999	Hela-S3	cervix:	n/a	chr11:59408837-59408848 chr11:59408839-59408848 chr11:59408839-59408846 chr11:59408838-59408847 chr11:59408839-59408847 chr11:59408837-59408849
47	JUND	chr11:59408679-59408999	HepG2	liver:	n/a	chr11:59408837-59408848 chr11:59408839-59408848 chr11:59408839-59408846 chr11:59408838-59408847 chr11:59408839-59408847 chr11:59408837-59408849
48	JUND	chr11:59415206-59415335	K562	blood:	n/a	n/a
49	MAFF	chr11:59410886-59411195	HepG2	liver:	n/a	n/a
50	MAFF	chr11:59397975-59398326	HepG2	liver:	n/a	chr11:59398155-59398173

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59405020-59405070	AoSMC	blood vessel:	n/a
2	chr11:59405020-59405070	HCF	heart:	n/a
3	chr11:59405020-59405070	ProgFib	skin:	n/a
4	chr11:59405020-59405070	T-47D	breast:	n/a
5	chr11:59405020-59405070	NHBE	bronchial:	n/a
6	chr11:59405020-59405070	BE2_C	brain:	n/a
7	chr11:59405020-59405070	Jurkat	blood:	n/a
8	chr11:59405020-59405070	SK-N-MC	brain:	n/a
9	chr11:59405020-59405070	RPTEC	kidney:	n/a
10	chr11:59405020-59405070	ECC-1	luminal epithelium:	n/a
11	chr11:59405020-59405070	AG04449	skin:	fetal
12	chr11:59405020-59405070	SKMC	muscle:	n/a
13	chr11:59405020-59405070	PFSK-1	brain:	n/a
14	chr11:59405020-59405070	AG04450	lung:	fetal
15	chr11:59405020-59405070	AG09319	gingival:	n/a
16	chr11:59405020-59405070	HepG2	liver:	n/a
17	chr11:59405020-59405070	HUVEC	blood vessel:	n/a
18	chr11:59405020-59405070	NHDF-neo	bronchial:	n/a
19	chr11:59405020-59405070	CMK	blood:	n/a
20	chr11:59405020-59405070	HCPEpiC	choroid plexus:	n/a
21	chr11:59405020-59405070	PrEC	prostate:	n/a
22	chr11:59405020-59405070	GM19239	blood:	n/a
23	chr11:59405020-59405070	HIPEpiC	eye:	n/a
24	chr11:59405020-59405070	Hepatocyte	liver:	n/a
25	chr11:59405020-59405070	HCM	heart:	n/a
26	chr11:59405020-59405070	A549	lung:	n/a
27	chr11:59405020-59405070	H1-hESC	embryonic stem cell:	embryo
28	chr11:59405020-59405070	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:59405020-59405070	Caco-2	colon:	n/a
30	chr11:59405020-59405070	HCT-116	colon:	n/a
31	chr11:59405020-59405070	MCF10A-Er-Src	breast:	n/a
32	chr11:59405020-59405070	HAEpiC	amniotic membrane:	n/a
33	chr11:59405020-59405070	Hela-S3	cervix:	n/a
34	chr11:59405020-59405070	GM12892	blood:	n/a
35	chr11:59405020-59405070	NB4	blood:	n/a
36	chr11:59405020-59405070	BJ	skin:	n/a
37	chr11:59405020-59405070	HMEC	breast:	n/a
38	chr11:59405020-59405070	SAEC	small airway:	n/a
39	chr11:59405020-59405070	HL-60	blood:	n/a
40	chr11:59405020-59405070	PANC-1	pancreas:	n/a
41	chr11:59405020-59405070	MCF-7	breast:	n/a
42	chr11:59405020-59405070	GM12891	blood:	n/a
43	chr11:59405020-59405070	GM06990	blood:	n/a
44	chr11:59405020-59405070	SK-N-SH	brain:	n/a
45	chr11:59405020-59405070	GM12878	blood:	n/a
46	chr11:59405020-59405070	HRPEpiC	eye:	n/a
47	chr11:59405020-59405070	K562	blood:	n/a
48	chr11:59405020-59405070	HEK293	kidney:	embryo
49	chr11:59405020-59405070	HRE	kidney:	n/a
50	chr11:59405020-59405070	HNPCEpiC	eye:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:59415544..59418168-chr11:59425035..59427737,3	K562	blood:
2	chr11:59424561..59426606-chr11:59430205..59433871,3	K562	blood:
3	chr11:59426718..59429219-chr11:59431171..59432816,2	MCF-7	breast:
4	chr11:59418234..59419771-chr11:59434112..59436530,2	K562	blood:
5	chr11:59383150..59385073-chr11:59402691..59405438,2	K562	blood:
6	chr11:59416984..59419803-chr11:59422236..59424673,2	K562	blood:
7	chr11:59424083..59426966-chr11:59434094..59436638,2	MCF-7	breast:
8	chr11:59396061..59398307-chr11:59402162..59404297,2	K562	blood:
9	chr11:59360123..59362224-chr11:59427629..59429741,2	K562	blood:
10	chr11:59430323..59433275-chr11:59435459..59437592,2	MCF-7	breast:
11	chr11:59400078..59402207-chr11:59435549..59437637,2	K562	blood:
12	chr11:59426478..59432385-chr11:59434040..59438268,6	K562	blood:
13	chr11:59424561..59426606-chr11:59430205..59433871,3	K562	blood:
14	chr11:59409381..59412375-chr11:59418263..59422142,3	K562	blood:
15	chr11:59413635..59416033-chr11:59418962..59421070,2	K562	blood:
16	chr11:59402868..59405539-chr11:59417059..59419661,2	K562	blood:
17	chr11:59402868..59406000-chr11:59417059..59419822,3	K562	blood:
18	chr11:59427815..59429405-chr11:59434904..59436653,2	MCF-7	breast:
19	chr11:59399439..59404169-chr11:59432679..59437637,5	K562	blood:
20	chr11:59379949..59382151-chr11:59418599..59421025,2	MCF-7	breast:
21	chr11:59415544..59418168-chr11:59425035..59427737,3	K562	blood:
22	chr11:59420045..59421714-chr11:59422885..59424724,2	K562	blood:
23	chr11:59418303..59420296-chr11:59422236..59424170,2	K562	blood:
24	chr11:59382222..59385204-chr11:59394078..59396704,2	K562	blood:
25	chr11:59416984..59419803-chr11:59422236..59424673,2	K562	blood:
26	chr11:59388045..59390986-chr11:59397842..59400769,2	K562	blood:
27	chr11:59420045..59421714-chr11:59422885..59424724,2	K562	blood:
28	chr11:59426691..59428934-chr11:59429924..59431970,2	K562	blood:
29	chr11:59406586..59408935-chr11:59435873..59437866,2	MCF-7	breast:
30	chr11:59382533..59384245-chr11:59402402..59404626,2	K562	blood:
31	chr11:59418303..59420296-chr11:59422236..59424170,2	K562	blood:
32	chr11:59409381..59412375-chr11:59418263..59422142,3	K562	blood:
33	chr11:59420557..59422154-chr11:59434243..59436764,2	MCF-7	breast:
34	chr11:59389914..59392610-chr11:59398281..59399870,2	K562	blood:
35	chr11:59402868..59405539-chr11:59417059..59419661,2	K562	blood:
36	chr11:59426691..59428934-chr11:59429924..59431970,2	K562	blood:
37	chr11:59381971..59384335-chr11:59420377..59423373,2	K562	blood:
38	chr11:59427010..59429204-chr11:59432808..59435498,2	MCF-7	breast:
39	chr11:59411267..59414686-chr11:59422826..59425210,4	K562	blood:
40	chr11:59402868..59406000-chr11:59417059..59419822,3	K562	blood:
41	chr11:59411267..59414686-chr11:59422826..59425210,4	K562	blood:
42	chr11:59396061..59398307-chr11:59402162..59404297,2	K562	blood:
43	chr11:59422509..59425773-chr11:59434045..59436546,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX3-2	chr11:59406793-59407334	ENSG00000255139.1
2	lnc-STX3-2	chr11:59406793-59407015	ENSG00000255139.1
3	lnc-STX3-2	chr11:59402893-59403009	NONHSAT021535
4	lnc-STX3-2	chr11:59402893-59403005	ENSG00000255139.1
5	lnc-STX3-2	chr11:59406793-59407121	NONHSAT021535

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PATL1	hsa-miR-19b-3p	chr11:59404525-59404518
2	PATL1	hsa-miR-19b-3p	chr11:59404962-59404989
3	PATL1	hsa-miR-19b-3p	chr11:59404968-59404961
4	PATL1	hsa-miR-19b-3p	chr11:59404519-59404541

Variant related genes	Relation type
PATL1	TF binding region
PATL1	CpG island
ENSG00000255355	chromatin interactions
ENSG00000255139	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000110048	chromatin interactions

Extended variants
information (count: 1233 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192980474	chr11:59396418-59396419	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201967719	chr11:59396425-59396426	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369666860	chr11:59396432-59396433	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs538951380	chr11:59396436-59396437	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs554480835	chr11:59396480-59396481	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs185158590	chr11:59396487-59396488	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188953526	chr11:59396490-59396491	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs555214002	chr11:59396522-59396523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112402318	chr11:59396536-59396537	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375010740	chr11:59396558-59396559	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs139806566	chr11:59396574-59396575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2186412	chr11:59396589-59396590	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs60249922	chr11:59396601-59396602	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2186413	chr11:59396631-59396632	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs558984321	chr11:59396633-59396634	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs577203202	chr11:59396672-59396673	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs149349734	chr11:59396706-59396707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559569963	chr11:59396709-59396710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147459748	chr11:59396759-59396760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541584115	chr11:59396825-59396826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563144122	chr11:59396851-59396852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530516555	chr11:59396852-59396853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551892162	chr11:59396890-59396891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563909177	chr11:59396906-59396907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142649006	chr11:59396951-59396952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528115249	chr11:59397015-59397016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535516286	chr11:59397031-59397032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546297403	chr11:59397116-59397117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566326215	chr11:59397296-59397297	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs181756977	chr11:59397303-59397304	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs117079104	chr11:59397322-59397323	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs570305868	chr11:59397441-59397442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537527973	chr11:59397468-59397469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554676947	chr11:59397506-59397507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186336944	chr11:59397525-59397526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577288539	chr11:59397575-59397576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563908094	chr11:59397600-59397601	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs140138986	chr11:59397663-59397664	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs528095419	chr11:59397709-59397710	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs574626782	chr11:59397751-59397752	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs541767461	chr11:59397800-59397801	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs80077858	chr11:59397818-59397819	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs60239171	chr11:59397825-59397826	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546689463	chr11:59397851-59397852	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs373243716	chr11:59397874-59397875	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs145683663	chr11:59397877-59397878	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs147710157	chr11:59397897-59397898	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs561578004	chr11:59397951-59397952	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs530410269	chr11:59397967-59397968	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs377669783	chr11:59397981-59397982	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59384400-59396600	Weak transcription	Fetal Thymus	thymus
2	chr11:59384400-59396800	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr11:59384400-59397400	Weak transcription	Adipose Nuclei	Adipose
4	chr11:59384400-59402600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr11:59384400-59404400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr11:59384800-59396800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:59384800-59396800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr11:59384800-59397000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr11:59384800-59397200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:59384800-59397200	Weak transcription	Liver	Liver
11	chr11:59384800-59402600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr11:59384800-59402800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr11:59384800-59404600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr11:59384800-59404800	Weak transcription	Brain Angular Gyrus	brain
15	chr11:59385000-59396600	Weak transcription	Primary T cells from cord blood	blood
16	chr11:59385000-59404400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr11:59385000-59404800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr11:59385400-59402800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr11:59385400-59402800	Weak transcription	Dnd41	blood
20	chr11:59385400-59403000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr11:59385400-59404200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr11:59385600-59403000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:59386600-59402800	Weak transcription	Placenta	Placenta
24	chr11:59390800-59397200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr11:59391200-59397400	Weak transcription	A549	lung
26	chr11:59391200-59402400	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr11:59391600-59397000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:59391800-59402200	Weak transcription	Primary B cells from cord blood	blood
29	chr11:59392000-59402600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:59392200-59397200	Weak transcription	Fetal Muscle Leg	muscle
31	chr11:59392200-59397200	Weak transcription	Osteobl	bone
32	chr11:59392400-59403600	Weak transcription	NHDF-Ad	bronchial
33	chr11:59392800-59402800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr11:59392800-59403000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:59392800-59403200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:59393000-59396600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr11:59393000-59402800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr11:59393200-59402600	Weak transcription	Primary hematopoietic stem cells	blood
39	chr11:59393200-59402600	Weak transcription	NHEK	skin
40	chr11:59393200-59404200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr11:59393400-59402600	Weak transcription	Spleen	Spleen
42	chr11:59393400-59402800	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr11:59393400-59403400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr11:59393600-59397000	Weak transcription	Fetal Muscle Trunk	muscle
45	chr11:59393600-59397400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:59393600-59402600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr11:59393600-59402800	Weak transcription	Fetal Intestine Large	intestine
48	chr11:59393600-59403200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr11:59393600-59403400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr11:59393600-59403600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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