Variant report

Variant	nsv430314
Chromosome Location	chr11:5411744-5496924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:793)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:5488057-5488184	K562	blood:	n/a	n/a
2	BACH1	chr11:5479355-5479376	K562	blood:	n/a	n/a
3	CCNT2	chr11:5482271-5482425	K562	blood:	n/a	n/a
4	CEBPB	chr11:5488104-5488204	H1-hESC	embryonic stem cell:	n/a	chr11:5488129-5488140
5	CEBPB	chr11:5465096-5465433	HepG2	liver:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
6	CEBPB	chr11:5487995-5488302	K562	blood:	n/a	chr11:5488129-5488140
7	CEBPB	chr11:5495409-5495560	K562	blood:	n/a	n/a
8	CEBPB	chr11:5488047-5488291	HepG2	liver:	n/a	chr11:5488129-5488140
9	CEBPB	chr11:5484600-5484903	HepG2	liver:	n/a	n/a
10	CEBPB	chr11:5465101-5465400	A549	lung:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
11	CEBPB	chr11:5465109-5465384	K562	blood:	n/a	chr11:5465270-5465283 chr11:5465270-5465281 chr11:5465269-5465286 chr11:5465270-5465283 chr11:5465270-5465283 chr11:5465271-5465282
12	CEBPB	chr11:5487417-5487661	K562	blood:	n/a	chr11:5487493-5487504 chr11:5487493-5487504
13	CHD2	chr11:5481680-5482514	K562	blood:	n/a	n/a
14	CREB1	chr11:5481891-5482945	K562	blood:	n/a	n/a
15	CREB1	chr11:5477763-5479678	K562	blood:	n/a	n/a
16	CTCF	chr11:5474040-5474330	HCT-116	colon:	n/a	n/a
17	CTCF	chr11:5411640-5411790	Caco-2	colon:	n/a	n/a
18	CTCF	chr11:5473908-5473936	Lung_OC	lung:	n/a	n/a
19	CTCF	chr11:5474060-5474210	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr11:5442341-5442440	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr11:5461914-5461956	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr11:5473960-5474110	WI-38	lung:	n/a	n/a
23	CTCF	chr11:5442260-5442410	Caco-2	colon:	n/a	n/a
24	CTCF	chr11:5495960-5496110	HPF	lung:	n/a	n/a
25	CTCF	chr11:5488940-5489090	GM12873	blood:	n/a	n/a
26	CTCF	chr11:5474060-5474210	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr11:5411600-5411750	NHLF	lung:	n/a	n/a
28	CTCF	chr11:5474000-5474150	HMF	breast:	n/a	n/a
29	CTCF	chr11:5442280-5442430	HCT-116	colon:	n/a	n/a
30	CTCF	chr11:5474080-5474230	AG04450	lung:	n/a	n/a
31	CTCF	chr11:5474022-5474269	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr11:5474000-5474150	GM12874	blood:	n/a	n/a
33	CTCF	chr11:5411680-5411830	A549	lung:	n/a	n/a
34	CTCF	chr11:5474080-5474230	HEK293	kidney:	n/a	n/a
35	CTCF	chr11:5474100-5474250	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr11:5442340-5442490	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr11:5474060-5474210	GM12867	blood:	n/a	n/a
38	CTCF	chr11:5411600-5411750	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr11:5474100-5474250	GM12872	blood:	n/a	n/a
40	CTCF	chr11:5473951-5474258	K562	blood:	n/a	n/a
41	CTCF	chr11:5442187-5442520	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr11:5474040-5474190	HCFaa	heart:	n/a	n/a
43	CTCF	chr11:5474134-5474180	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:5461880-5461993	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:5474120-5474270	K562	blood:	n/a	n/a
46	CTCF	chr11:5474100-5474250	GM12864	blood:	n/a	n/a
47	CTCF	chr11:5462680-5462830	Caco-2	colon:	n/a	n/a
48	CTCF	chr11:5432429-5432471	Medullo	brain:	n/a	n/a
49	CTCF	chr11:5474080-5474230	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:5474020-5474170	AG04450	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5442443-5442493	ovcar-3	ovarian:	n/a
2	chr11:5474584-5474634	NH-A	brain:	n/a
3	chr11:5462916-5462966	AG04449	skin:	fetal
4	chr11:5442443-5442493	GM12878	blood:	n/a
5	chr11:5442443-5442493	HCT-116	colon:	n/a
6	chr11:5474965-5475015	H1-hESC	embryonic stem cell:	embryo
7	chr11:5442434-5442484	HepG2	liver:	n/a
8	chr11:5474584-5474634	HEEpiC	esophagus:	n/a
9	chr11:5475082-5475132	PANC-1	pancreas:	n/a
10	chr11:5463768-5463818	HEEpiC	esophagus:	n/a
11	chr11:5442443-5442493	HRE	kidney:	n/a
12	chr11:5462916-5462966	A549	lung:	n/a
13	chr11:5474584-5474634	AG04449	skin:	fetal
14	chr11:5442511-5442561	PFSK-1	brain:	n/a
15	chr11:5442434-5442484	HIPEpiC	eye:	n/a
16	chr11:5474584-5474634	HUVEC	blood vessel:	n/a
17	chr11:5442434-5442484	MCF10A-Er-Src	breast:	n/a
18	chr11:5433817-5433867	MCF-7	breast:	n/a
19	chr11:5442434-5442484	K562	blood:	n/a
20	chr11:5442511-5442561	SK-N-SH_RA	brain:	n/a
21	chr11:5442434-5442484	BJ	skin:	n/a
22	chr11:5463768-5463818	HRPEpiC	eye:	n/a
23	chr11:5462916-5462966	HCT-116	colon:	n/a
24	chr11:5474584-5474634	LNCaP	prostate:	n/a
25	chr11:5444223-5444273	PrEC	prostate:	n/a
26	chr11:5442443-5442493	BJ	skin:	n/a
27	chr11:5474584-5474634	HCF	heart:	n/a
28	chr11:5474965-5475015	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:5463768-5463818	HRCEpiC	kidney:	n/a
30	chr11:5463768-5463818	PFSK-1	brain:	n/a
31	chr11:5462540-5462590	ECC-1	luminal epithelium:	n/a
32	chr11:5433817-5433867	NHDF-neo	bronchial:	n/a
33	chr11:5444223-5444273	HIPEpiC	eye:	n/a
34	chr11:5444223-5444273	HMEC	breast:	n/a
35	chr11:5463768-5463818	IMR90	lung:	fetal
36	chr11:5474001-5474051	GM19239	blood:	n/a
37	chr11:5474612-5474662	Caco-2	colon:	n/a
38	chr11:5474612-5474662	SKMC	muscle:	n/a
39	chr11:5463768-5463818	AG09309	skin:	n/a
40	chr11:5442443-5442493	ECC-1	luminal epithelium:	n/a
41	chr11:5442443-5442493	PrEC	prostate:	n/a
42	chr11:5475082-5475132	Caco-2	colon:	n/a
43	chr11:5474612-5474662	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:5474001-5474051	LNCaP	prostate:	n/a
45	chr11:5442434-5442484	A549	lung:	n/a
46	chr11:5442443-5442493	BE2_C	brain:	n/a
47	chr11:5474584-5474634	HEK293	kidney:	embryo
48	chr11:5475082-5475132	ProgFib	skin:	n/a
49	chr11:5463768-5463818	NB4	blood:	n/a
50	chr11:5474965-5475015	LNCaP	prostate:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:5146608-5154908..11:5482799-5488942	H1-hESC	embryonic stem cell:	embryo
2	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
3	11:5475173-5482799..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
4	chr11:5486296..5490583-chr11:5492213..5495535,7	K562	blood:
5	chr11:5330393..5334206-chr11:5464650..5469323,6	K562	blood:
6	11:5482799-5488942..11:5533869-5541626	Hela-S3	cervix:
7	11:5218976-5222789..11:5425882-5426881	GM12878	blood:
8	11:5494633-5496671..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
9	11:4778081-4789138..11:5425882-5426881	H1-hESC	embryonic stem cell:	embryo
10	chr11:5454190..5457946-chr11:5459430..5461152,3	K562	blood:
11	11:5475173-5482799..11:5714465-5718134	H1-hESC	embryonic stem cell:	embryo
12	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
13	chr11:5486296..5490583-chr11:5492213..5495535,7	K562	blood:
14	chr11:5487225..5489832-chr11:5524336..5528064,4	K562	blood:
15	11:5482799-5488942..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
16	11:5146608-5154908..11:5469052-5469844	H1-hESC	embryonic stem cell:	embryo
17	11:5146608-5154908..11:5475173-5482799	GM12878	blood:
18	chr11:5473913..5477314-chr11:5481378..5484455,3	K562	blood:
19	11:5482799-5488942..11:5707362-5712027	H1-hESC	embryonic stem cell:	embryo
20	11:5250847-5268367..11:5463864-5469052	K562	blood:
21	chr11:5494329..5498413-chr11:5524095..5528083,5	K562	blood:
22	11:4778081-4789138..11:5482799-5488942	Hela-S3	cervix:
23	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:
24	chr11:5468259..5472386-chr11:5473307..5476028,4	K562	blood:
25	11:5482799-5488942..11:5721056-5732713	Hela-S3	cervix:
26	11:5488942-5494633..11:5721056-5732713	H1-hESC	embryonic stem cell:	embryo
27	chr11:5452403..5455534-chr11:5455885..5459349,3	K562	blood:
28	11:4988858-5002113..11:5469844-5475173	Hela-S3	cervix:
29	11:5407716-5412355..11:5482799-5488942	H1-hESC	embryonic stem cell:	embryo
30	11:5421776-5424121..11:5425882-5426881	GM12878	blood:
31	chr11:5413872..5415694-chr11:5419975..5421750,2	K562	blood:
32	11:5482799-5488942..11:5527719-5533869	H1-hESC	embryonic stem cell:	embryo
33	chr11:5492399..5493944-chr11:5512243..5514587,2	K562	blood:
34	11:5321718-5325668..11:5463864-5469052	K562	blood:
35	chr11:5495751..5498334-chr11:5524095..5527159,4	K562	blood:
36	chr11:5415584..5416428-chr20:41864268..41865032,2	MCF-7	breast:
37	chr11:5492428..5495809-chr11:5496479..5499256,6	K562	blood:
38	11:5250847-5268367..11:5482799-5488942	Hela-S3	cervix:
39	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
40	chr11:5402054..5402614-chr11:5441811..5442439,2	MCF-7	breast:
41	11:5460021-5463864..11:5469052-5469844	H1-hESC	embryonic stem cell:	embryo
42	chr11:5448582..5452295-chr11:5454742..5458081,4	K562	blood:
43	chr11:5442840..5444659-chr11:5449789..5452716,3	K562	blood:
44	chr11:5495902..5498056-chr11:5528624..5530826,2	K562	blood:
45	chr11:5492428..5495809-chr11:5496479..5499256,6	K562	blood:
46	11:5243048-5250847..11:5425882-5426881	GM12878	blood:
47	chr11:5486174..5488915-chr11:5526268..5527984,3	K562	blood:
48	chr11:5454551..5456372-chr11:5525349..5527757,2	K562	blood:
49	11:5482799-5488942..11:5714465-5718134	Hela-S3	cervix:
50	chr11:5438689..5441571-chr11:5444297..5446358,2	K562	blood:

No data

Variant related genes	Relation type
OR51I2	TF binding region
OR51I1	TF binding region
OR51K1P	TF binding region
OR51A10P	TF binding region
OR51J1	TF binding region
OR51Q1	TF binding region
OR51I2	CpG island
OR51I1	CpG island
OR51K1P	CpG island
OR51A10P	CpG island
OR51J1	CpG island
OR51Q1	CpG island
ENSG00000229988	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000248424	chromatin interactions
ENSG00000167360	chromatin interactions
ENSG00000167346	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000184698	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000181616	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000167359	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000184321	chromatin interactions

Extended variants
information (count: 4464 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:4464 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7395908	chr11:5411744-5411745	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556443590	chr11:5411745-5411746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7395910	chr11:5411796-5411797	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs545028059	chr11:5411801-5411802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369050089	chr11:5411812-5411813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs61892014	chr11:5411883-5411884	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs188387012	chr11:5411920-5411921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2736530	chr11:5411934-5411935	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs145050521	chr11:5411992-5411993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367590734	chr11:5411993-5411994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2340320	chr11:5412038-5412039	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs550967363	chr11:5412044-5412045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569566105	chr11:5412046-5412047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2340321	chr11:5412059-5412060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs11037191	chr11:5412072-5412073	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs76545626	chr11:5412124-5412125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543677800	chr11:5412130-5412131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377226341	chr11:5412167-5412168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567097298	chr11:5412190-5412191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538073094	chr11:5412233-5412234	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182025024	chr11:5412248-5412249	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2340322	chr11:5412289-5412290	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs2879737	chr11:5412297-5412298	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs553760554	chr11:5412347-5412348	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7395015	chr11:5412374-5412375	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs16930388	chr11:5412385-5412386	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138897935	chr11:5412387-5412388	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547517121	chr11:5412405-5412406	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187239463	chr11:5412422-5412423	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544829499	chr11:5412427-5412428	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114902465	chr11:5412450-5412451	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371249060	chr11:5412453-5412454	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192030712	chr11:5412454-5412455	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183473933	chr11:5412493-5412494	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35940333	chr11:5412517-5412518	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11037193	chr11:5412543-5412544	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs549046274	chr11:5412571-5412572	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11037194	chr11:5412591-5412592	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs11037195	chr11:5412598-5412599	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549899863	chr11:5412654-5412655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571362547	chr11:5412671-5412672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11037196	chr11:5412684-5412685	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs11037197	chr11:5412698-5412699	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs558498984	chr11:5412720-5412721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115744188	chr11:5412766-5412767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186792166	chr11:5412774-5412775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368834335	chr11:5412788-5412789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576135737	chr11:5412796-5412797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543157843	chr11:5412820-5412821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190071339	chr11:5412863-5412864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5409600-5412200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:5410600-5412600	Strong transcription	K562	blood
3	chr11:5412200-5412400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:5412600-5415000	Weak transcription	K562	blood
5	chr11:5415000-5417000	Strong transcription	K562	blood
6	chr11:5415800-5417000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:5417000-5417400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:5417000-5420000	Weak transcription	K562	blood
9	chr11:5417400-5420800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:5420000-5423000	Strong transcription	K562	blood
11	chr11:5420800-5421000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:5422000-5422200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:5423000-5424200	Weak transcription	K562	blood
14	chr11:5424200-5425800	Strong transcription	K562	blood
15	chr11:5425800-5432400	Weak transcription	K562	blood
16	chr11:5429600-5430000	Enhancers	Fetal Kidney	kidney
17	chr11:5432400-5433400	Enhancers	K562	blood
18	chr11:5433000-5433400	Enhancers	Hela-S3	cervix
19	chr11:5433200-5433600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr11:5433200-5433800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr11:5433400-5433600	Flanking Active TSS	K562	blood
22	chr11:5433400-5433800	Active TSS	A549	lung
23	chr11:5433600-5433800	Active TSS	K562	blood
24	chr11:5433600-5434000	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr11:5433800-5434400	Enhancers	K562	blood
26	chr11:5434400-5440400	Weak transcription	K562	blood
27	chr11:5440400-5441200	Strong transcription	K562	blood
28	chr11:5441200-5442400	Weak transcription	K562	blood
29	chr11:5442400-5444400	Strong transcription	K562	blood
30	chr11:5444000-5445000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr11:5444400-5447000	Weak transcription	K562	blood
32	chr11:5445000-5445200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr11:5445200-5445600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr11:5445400-5446000	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr11:5445600-5448400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:5446800-5447200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:5447000-5448800	Strong transcription	K562	blood
38	chr11:5447200-5447800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:5447800-5448000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:5448000-5448200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:5448200-5448400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:5448400-5448600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr11:5448400-5448600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:5448600-5449000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:5448800-5450000	Weak transcription	K562	blood
46	chr11:5449000-5451400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:5450000-5450800	Genic enhancers	K562	blood
48	chr11:5450400-5450800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:5450800-5453400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:5450800-5458800	Strong transcription	K562	blood

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